Mumbai, Maharashtra
GST No. 27AAFFH3493R3ZK
Approx. Rs 281.25 / VialGet Latest Price
Product Details:| Strength | 50 mg |
| Formulation Type | Liposomal |
| Form Of Medicine | Powder |
| Brand | Celon Labs |
| Manufacturer | Celon Laboratories |
| Storage Condition | Refrigerate (2-8°C) |
| Shelf Life | 18 months |
| Pharmacopoeia Standard | IP |
| Packaging Size | 2 ml |
| Composition | Doxorubicin Hydrochloride |
Healthy Inc offers Doxorubicin Hydrochloride, a potent Anthracycline Cytotoxic Antibiotic and a cornerstone of modern oncology. This ready-to-use liquid formulation (50 mg in 25 ml) works by intercalating DNA and inhibiting Topoisomerase II, effectively halting the proliferation of malignant cells. It is a clinical priority for treating Acute Leukemias, Soft Tissue Sarcomas, Hodgkin’s and Non-Hodgkin’s Lymphomas, and solid tumors including Breast, Ovarian, and Bladder cancers. As a leading Indian export partner, we supply these high-criticality oncology injectables to specialized cancer centers and hospital networks worldwide.
Manufacturing: Produced in associated WHO-GMP specialized oncology units, ensuring 100% sterility, zero cross-contamination, and strict adherence to Indian Pharmacopoeia (IP) standards for cytotoxic liquids.
Climate Stability: Validated for Zone IVb (Hot/Humid) conditions; the formulation is stabilized to maintain molecular integrity and prevent degradation during transit to Africa, LATAM, and SEA markets.
Regulatory Support: Full technical documentation available, including CTD/eCTD Dossiers and specialized Material Safety Data Sheets (MSDS) to streamline the registration of high-potency therapeutics.
Accepting B2B inquiries for contract manufacturing, bulk supply, and global distribution partnerships from our Mumbai export hub.
Available strengths and quality? We supply Doxorubicin in 25 ml vials (2 mg/ml, totaling 50 mg). Every batch undergoes rigorous HPLC-based assay testing, sterility validation, and Bacterial Endotoxin Testing (BET) to meet international safety profiles for intravenous infusion.
Support for tropical export? Yes. Doxorubicin is light-sensitive and requires careful thermal management. Our product is Zone IVb stability-tested, utilizing amber-colored USP Type I glass vials and light-protective secondary packaging to ensure the molecule remains stable during international shipping.
Registration assistance provided? We provide complete Regulatory Technical Files (CTD) and Certificates of Analysis (COA) to facilitate local health authority approvals and oncology tender participations in your specific region.
Small-volume or mixed orders? We specialize in mixed-container consolidation, allowing you to combine Doxorubicin 50 mg with other oncology agents (such as Docetaxel or Cisplatin), supportive care injectables, and specialized antibiotics in a single, cost-effective shipment.
Direct sourcing? Products are sourced through Healthy Life Group’s associated WHO-GMP specialized manufacturing units, ensuring competitive direct-from-factory pricing and strict quality control oversight for hazardous drug handling.
Approx. Rs 3.75 / PieceGet Latest Price
Product Details:| Strength | 25 mg/ml |
| Pack Size | 1 ml |
| Pack Type | Ampoule |
| Prescription | Prescription |
| Form | Injection |
| Usage | IM Use |
| Shelf Life | 12 months |
| Country of Origin | India |
Healthy Inc offers this synergistic Bronchodilator combination, a clinical cornerstone for the management of reversible airway obstruction. Formulated with Etophylline (a stable derivative of Theophylline) and Theophylline anhydrous, this injection works by relaxing the smooth muscles of the bronchial airways and pulmonary blood vessels. It is a frontline therapeutic for Bronchial Asthma, Chronic Obstructive Pulmonary Disease (COPD), Status Asthmaticus, and Left Ventricular Failure (Cardiac Asthma). As a specialized Indian export partner, we provide these essential respiratory solutions to hospital networks and emergency clinics in global pharmaceutical markets.
Manufacturing: Produced in associated WHO-GMP certified sterile facilities, ensuring 100% sterility, precise ratio accuracy, and high molecular purity for Intramuscular (IM) or slow Intravenous (IV) administration.
Climate Stability: Validated for Zone IVb (Hot/Humid) conditions, ensuring the xanthine derivatives remain stable and potent across the tropical climates of Africa, LATAM, and SEA markets.
Regulatory Support: Full technical documentation available, including CTD/eCTD Dossiers, to streamline the registration process and meet local health authority requirements.
Accepting B2B inquiries for contract manufacturing, bulk supply, and global distribution partnerships from our Mumbai export hub.
Available strengths and quality? We supply this combination in 2 ml ampoules containing 169.4 mg Etophylline and 50.6 mg Theophylline. Every batch undergoes rigorous HPLC-based assay testing, sterility validation, and pH stability checks to meet international pharmacopoeia standards.
Support for tropical export? Yes. Our formulation is Zone IVb stability-tested. We utilize neutral USP Type I glass ampoules and specialized export-grade secondary packaging to prevent chemical degradation during international transit to high-temperature and high-humidity regions.
Registration assistance provided? We provide complete Regulatory Technical Files (CTD) and Certificates of Analysis (COA) to facilitate local health authority approvals and government hospital tender participations in your specific territory.
Small-volume or mixed orders? We specialize in mixed-container consolidation, allowing you to combine this respiratory injection with other therapeutic categories (such as Corticosteroids like Dexamethasone, Antibiotics, or IV fluids) in a single, cost-effective shipment to optimize your inventory.
Direct manufacturing? Products are sourced through Healthy Life Group’s associated WHO-GMP manufacturing units, ensuring competitive direct-from-factory pricing and strict quality control oversight.
Approx. Rs 92.82 / VialGet Latest Price
Product Details:| Strength | 100 mg |
| Brand | Posid |
| Treatment | Small Cell Lung Cancer |
| Packaging Type | Vial |
| Manufacturer | Fresenius Kabi |
| Storage | 2 to 8 degree c |
| Dosage Form | Concentrate for Solution for Infusion |
| Shelf Life | 24 Months |
| Pharmacopoeia Standard | IP |
| Vial Size | 5 ml |
| Composition | Etoposide |
Healthy Inc offers Etoposide 100 mg, a high-potency Topoisomerase II inhibitor and a vital component in multi-drug chemotherapy regimens. Etoposide works by causing DNA strand breaks, effectively preventing malignant cells from entering mitosis. It is a clinical priority for the treatment of Small Cell Lung Cancer (SCLC), Refractory Testicular Tumors, Acute Myeloid Leukemia (AML), and Lymphomas. As a specialized Indian export partner, we supply these high-criticality oncology solutions to specialized cancer institutes and hospital networks in global pharmaceutical markets.
Manufacturing: Produced in associated WHO-GMP certified oncology-dedicated sterile facilities, ensuring 100% sterility, zero cross-contamination, and strict adherence to Indian Pharmacopoeia (IP) standards for hazardous drug handling.
Climate Stability: Validated for Zone IVb (Hot/Humid) conditions; the formulation is stabilized in a non-aqueous solvent system to maintain chemical integrity across Africa, LATAM, and SEA markets.
Regulatory Support: Full technical documentation available, including CTD/eCTD Dossiers and specialized handling protocols, to streamline the registration of cytotoxic therapeutics.
Accepting B2B inquiries for contract manufacturing, bulk supply, and global distribution partnerships from our Mumbai export hub.
Available strengths and quality? We supply Etoposide as a sterile concentrated solution in 5 ml vials containing 100 mg (20 mg/ml). Every batch undergoes rigorous HPLC-based assay testing, sterility validation, and Bacterial Endotoxin Testing (BET) to ensure the highest safety profile for slow intravenous infusion.
Support for tropical export? Yes. Etoposide requires careful storage to prevent degradation. Our product is Zone IVb stability-tested, utilizing neutral USP Type I glass vials and specialized export-grade secondary packaging to ensure molecular stability during international transit to high-temperature regions.
Registration assistance provided? We provide complete Regulatory Technical Files (CTD) and Certificates of Analysis (COA) to facilitate local health authority approvals and oncology tender participations in your specific territory.
Small-volume or mixed orders? We specialize in mixed-container consolidation, allowing you to combine Etoposide with other oncology agents (such as Cisplatin, Carboplatin, or Docetaxel), supportive care injectables, and specialized antibiotics in a single, cost-effective shipment.
Direct manufacturing? Products are sourced through Healthy Life Group’s associated WHO-GMP specialized manufacturing units, ensuring competitive direct-from-factory pricing and strict quality control oversight for high-potency antineoplastic therapies.
Approx. Rs 2.82 / BoxGet Latest Price
Product Details:| Route Of Administration | IM and IV |
| Brand | Lasix |
| Strength | 10 mg |
| Vial Volume | 2 ml |
| Container Type | Vial |
| Pack Quantity | 4 vials |
| Pharmacopoeia Standard | IP |
| Shelf Life | 24 months |
| Treatment | Kidney Disease |
| Composition | Furosemide |
Healthy Inc offers Frusemide (also known as Furosemide), a high-potency Loop Diuretic and a critical component in emergency and fluid-management medicine. Frusemide is the clinical gold standard for achieving rapid diuresis by inhibiting sodium and chloride reabsorption in the kidneys. It is a frontline therapeutic for Acute Pulmonary Edema, Congestive Heart Failure (CHF), Hypertensive Crises, and edema associated with hepatic or renal disease. As a specialized Indian export partner, we supply this essential diuretic to ICU networks, cardiology units, and emergency departments in global pharmaceutical markets.
Manufacturing: Produced in associated WHO-GMP certified sterile facilities, ensuring 100% sterility, high molecular purity, and precise 10 mg/ml concentration for Intramuscular (IM) or Intravenous (IV) administration.
Climate Stability: Validated for Zone IVb (Hot/Humid) conditions, ensuring the Frusemide molecule remains stable and potent across the tropical climates of Africa, LATAM, and SEA markets.
Regulatory Support: Full technical documentation available, including CTD/eCTD Dossiers, to streamline the registration process for essential critical-care injectables.
Accepting B2B inquiries for contract manufacturing, bulk supply, and global distribution partnerships from our Mumbai export hub.
Available strengths and packaging? We supply Frusemide in the standard 10 mg/ml concentration, typically available in 2 ml ampoules (20 mg) or larger multi-dose vials for hospital use. Every batch undergoes rigorous HPLC-based assay testing and sterility validation to meet Indian Pharmacopoeia (IP) and international standards.
Support for tropical export? Yes. Frusemide is light-sensitive and prone to degradation if not handled correctly. Our formulation is Zone IVb stability-tested, utilizing amber USP Type I glass ampoules and specialized light-protective secondary packaging to ensure product integrity during international transit.
Registration assistance provided? We provide complete Regulatory Technical Files (CTD) and Certificates of Analysis (COA) to facilitate local health authority approvals and government hospital tender participations in your specific region.
Small-volume or mixed orders? We specialize in mixed-container consolidation, allowing you to combine Frusemide with other critical care injectables (such as Dopamine, Epinephrine, or cardiovascular medicines) and IV fluids in a single, cost-effective shipment.
Direct sourcing? Products are sourced through Healthy Life Group’s associated WHO-GMP manufacturing units, ensuring competitive direct-from-factory pricing and strict quality control oversight for essential diuretic therapies.
Approx. Rs 80.00 / PieceGet Latest Price
Product Details:| Strength | 50 mcg/ml |
| Dosage Form | Injection |
| Pack Size | 1 ml |
| Storage | 2–8°C |
| Route | IV |
| Usage | Hospital |
| Brand | Sandostatin |
| Shelf Life | 18 months |
Healthy Inc offers Octreotide Injection, a highly potent synthetic Somatostatin Analogue. Containing Octreotide Acetate 50 mcg, this formulation is a clinical priority for the pharmacological management of gastrointestinal and endocrine disorders. It is a frontline therapeutic for suppressing the severe diarrhea and flushing associated with Metastatic Carcinoid Tumors and VIPomas. Additionally, it is utilized for the treatment of Acromegaly in patients who have had an inadequate response to other therapies. As a specialized Indian export partner, we supply this essential peptide therapeutic to endocrinology units and gastroenterology centers in global pharmaceutical markets.
Pharmacological Precision: Provides more potent inhibition of growth hormone, glucagon, and insulin than natural somatostatin, with a significantly longer duration of action. It is also utilized in emergency protocols for Acute Variceal Bleeding to reduce splanchnic blood flow.
Manufacturing: Produced in associated WHO-GMP certified sterile facilities. The process ensures 100% sterility, high molecular purity, and a precise 50 mcg/mL concentration for Subcutaneous (SC) or Intravenous (IV) administration.
Climate Stability: Validated for Zone IVb (Hot/Humid) conditions. While refrigerated storage (2∘C to 8∘C) is recommended for long-term stability, our formulation is stabilized to maintain integrity during global transit across Africa, LATAM, and SEA markets.
Regulatory Support: Full technical documentation available, including CTD/eCTD Dossiers, to streamline the registration of specialized hormonal and critical-care therapeutics.
Accepting B2B inquiries for contract manufacturing, bulk supply, and global distribution partnerships from our Mumbai export hub.
Available strengths and packaging? We supply Octreotide in 1 mL ampoules or vials at the 50 mcg strength, as well as 100 mcg and 500 mcg concentrations. Every batch undergoes rigorous HPLC-based assay testing and Bacterial Endotoxin Testing (BET) to meet international standards.
Support for tropical export? Yes. Octreotide is a temperature-sensitive peptide. Our product is Zone IVb stability-tested, and we utilize specialized thermal-insulated shipping containers and cold-chain logistics to maintain product efficacy during international transit to high-temperature regions.
Registration assistance provided? We provide complete Regulatory Technical Files (CTD) and Certificates of Analysis (COA) to facilitate local health authority approvals and government healthcare tender participations in your specific territory.
Small-volume or mixed orders? We specialize in mixed-container consolidation, allowing you to combine Octreotide 50 mcg with other critical care injectables (such as Terlipressin, Pantoprazole, or various emergency medications) in a single, cost-effective shipment.
Direct sourcing? Products are sourced through Healthy Life Group’s associated WHO-GMP specialized manufacturing units, ensuring competitive direct-from-factory pricing and strict quality control oversight for advanced hormonal therapies.
Approx. Rs 4.13 / PieceGet Latest Price
Product Details:| Strength | 2 mg/ml |
| Pack size | 2 ml |
| Brand | Cipla |
| Pack type | Ampoule |
| Route | IV |
| Prescription | Rx only |
| Shelf life | 24 months |
| Dosage form | Injection |
| Composition | Ondansetron |
Healthy Inc offers Ondansetron Injection IP, a highly effective 5-HT₃ Receptor Antagonist and the gold standard in antiemetic therapy. Containing Ondansetron 2 mg per mL, this formulation is a clinical priority for the prevention and management of Nausea and Vomiting induced by highly emetogenic chemotherapy, radiotherapy, and post-operative recovery. As a specialized Indian export partner, we supply this essential supportive-care therapeutic to oncology centers, surgical units, and emergency departments across global pharmaceutical markets.
Clinical Precision: Acts through highly selective antagonism of serotonin receptors in both the peripheral vagus nerve terminals and the central Chemoreceptor Trigger Zone (CTZ), providing rapid relief without the sedative or extrapyramidal side effects associated with older antiemetics.
Manufacturing: Produced in associated WHO-GMP certified sterile facilities. The solution is formulated under strict aseptic conditions to ensure 100% sterility, high molecular purity, and precise pH balance for Intravenous (IV) or Intramuscular (IM) administration.
Climate Stability: Validated for Zone IVb (Hot/Humid) conditions; the formulation is stabilized to prevent photodegradation and ensure chemical integrity across Africa, LATAM, and SEA markets.
Regulatory Support: Full technical documentation available, including CTD/eCTD Dossiers, to streamline the registration of essential supportive care and hospital-grade therapeutics.
Accepting B2B inquiries for contract manufacturing, bulk supply, and global distribution partnerships from our Mumbai export hub.
Available strengths and packaging? We supply Ondansetron in the standard 2 mg / mL concentration, available in 2 mL ampoules (4 mg) and 4 mL ampoules (8 mg). Every batch undergoes rigorous HPLC-based assay testing and sterility validation to meet Indian Pharmacopoeia (IP) and international standards.
Support for tropical export? Yes. Our formulation is Zone IVb stability-tested. We utilize neutral USP Type I glass ampoules and moisture-resistant secondary packaging to ensure the product remains stable during international transit to high-temperature regions.
Registration assistance provided? We provide complete Regulatory Technical Files (CTD) and Certificates of Analysis (COA) to facilitate local health authority approvals and government healthcare or oncology tender participations in your specific territory.
Small-volume or mixed orders? We specialize in mixed-container consolidation, allowing you to combine Ondansetron with other gastrointestinal or critical care injectables (such as Pantoprazole, Dexamethasone, or Metoclopramide) in a single, cost-effective shipment.
Direct sourcing? Products are sourced through Healthy Life Group’s associated WHO-GMP manufacturing units, ensuring competitive direct-from-factory pricing and strict quality control oversight for essential antiemetic care.
Approx. Rs 2,165.63 / VialGet Latest Price
Product Details:| Dosage Form | Injection |
| Strength | 500 mg |
| Treatment | Non-Small Cell Lung Cancer |
| Manufacturer | Natco Pharma |
| Brand Name | Alimta |
| Pharmacopoeia Standard | IP |
| Salt Form | Disodium |
| Shelf Life | 24 months |
| Storage Temperature | 2-8 degree c |
| Composition | Pemetrexed |
Healthy Inc offers Pemetrexed Injection IP, a high-potency Multitargeted Antifolate Antineoplastic agent essential for advanced oncology protocols. Containing Pemetrexed Disodium 500 mg, this formulation is a clinical priority for the treatment of Malignant Pleural Mesothelioma and serves as a cornerstone frontline or maintenance therapy for Locally Advanced or Metastatic Non-Squamous Non-Small Cell Lung Cancer (NSCLC). As a specialized Indian export partner, we supply this critical cytotoxic injectable to oncology hospitals and specialized infusion centers in global pharmaceutical markets.
Advanced Mechanism of Action: Distinct from traditional antifolates, Pemetrexed simultaneously inhibits three key enzymes—thymidylate synthase (TS), dihydrofolate reductase (DHFR), and glycinamide ribonucleotide formyltransferase (GARFT). This triple-action inhibition effectively halts the purine and pyrimidine synthesis required for cancer cell DNA/RNA replication.
Manufacturing Excellence: Produced in associated WHO-GMP certified specialized oncology facilities. The Lyophilized Powder presentation ensures 100% sterility, high molecular purity, and rapid, residue-free reconstitution for Intravenous (IV) infusion.
Clinical Safety Support: Our technical dossiers emphasize the required premedication protocols (Folic Acid, Vitamin B12, and Corticosteroids) to mitigate hematologic and gastrointestinal toxicities, supporting clinical teams in international territories.
Climate Stability: Validated for Zone IVb (Hot/Humid) conditions. The freeze-dried lyophilized cake is engineered for maximum stability, ensuring potency and chemical integrity across the tropical climates of Africa, LATAM, and SEA markets.
Accepting B2B inquiries for contract manufacturing, bulk supply, and oncology distribution partnerships from our Mumbai export hub.
Available strengths and packaging? We supply Pemetrexed in the 500 mg vial and the 100 mg vial. Each 500 mg vial is intended for single-dose use and undergoes rigorous HPLC-based assay testing, sterility validation, and Bacterial Endotoxin Testing (BET) to meet Indian Pharmacopoeia (IP) and international standards.
Support for tropical export? Yes. Pemetrexed 500 mg is Zone IVb stability-tested. We utilize neutral USP Type I glass vials and moisture-resistant, light-shielding secondary packaging to protect the cytotoxic agent during international transit and storage in high-temperature regions.
Registration assistance provided? We provide complete Regulatory Technical Files (CTD) and Certificates of Analysis (COA) to facilitate local health authority approvals and government oncology tender participations in your specific territory.
Small-volume or mixed orders? We specialize in mixed-container consolidation, allowing you to combine Pemetrexed 500 mg with other oncology essentials (such as Cisplatin, Carboplatin, or supportive care injectables like Ondansetron and Dexamethasone) in a single, cost-effective shipment.
Direct sourcing? Products are sourced through Healthy Life Group’s associated WHO-GMP oncology manufacturing units, ensuring competitive direct-from-factory pricing and strict quality control oversight for advanced chemotherapy treatments.
Approx. Rs 2.82 / VialGet Latest Price
Product Details:| Strength | 25 mg/ml |
| Pack Size | 2 ml |
| Brand | Phenergan |
| Pack Type | Ampoule |
| Route | IM |
| Prescription Type | Prescription |
| Usage | Allergy |
Healthy Inc offers Promethazine Hydrochloride Injection IP, a highly versatile Phenothiazine-derivative Antihistamine and antiemetic. Containing 25 mg per mL, this formulation is a clinical priority for the rapid management of acute allergic reactions, the prevention and control of nausea and vomiting associated with anesthesia or surgery, and as an adjunct to analgesics for post-operative pain. As a specialized Indian export partner, we supply this essential therapeutic to emergency departments, surgical units, and general hospitals in global pharmaceutical markets.
Multi-Action Efficacy: Acts as a potent H₁ receptor antagonist to alleviate allergic symptoms, while also possessing significant antiemetic, sedative, and anticholinergic properties. Its rapid onset when administered via Deep Intramuscular (IM) or slow Intravenous (IV) routes makes it a frontline choice for acute symptomatic relief.
Manufacturing Excellence: Produced in associated WHO-GMP certified sterile facilities. The solution is formulated under strict aseptic conditions to ensure 100% sterility, high molecular purity, and precise pH balance to maintain stability and patient safety.
Climate Stability: Validated for Zone IVb (Hot/Humid) conditions; the formulation is stabilized and protected against photodegradation to ensure chemical integrity across Africa, LATAM, and SEA markets.
Regulatory Support: Full technical documentation available, including CTD/eCTD Dossiers, to streamline the registration of essential sedative and antiemetic therapeutics.
Accepting B2B inquiries for contract manufacturing, bulk supply, and global distribution partnerships from our Mumbai export hub.
Available strengths and packaging? We supply Promethazine Hydrochloride in the standard 25 mg / mL and 50 mg / 2 mL concentrations, typically in 1 mL or 2 mL amber USP Type I ampoules. Every batch undergoes rigorous HPLC-based assay testing and sterility validation to meet Indian Pharmacopoeia (IP) standards.
Support for tropical export? Yes. Our formulation is Zone IVb stability-tested. We utilize amber glass ampoules and light-shielding secondary packaging to protect the Promethazine molecule from UV degradation and thermal instability during international transit.
Registration assistance provided? We provide complete Regulatory Technical Files (CTD) and Certificates of Analysis (COA) to facilitate local health authority approvals and government healthcare or surgical tender participations in your specific territory.
Small-volume or mixed orders? We specialize in mixed-container consolidation, allowing you to combine Promethazine with other emergency or surgical essentials (such as Ondansetron, Dexamethasone, or Diclofenac) in a single, cost-effective shipment.
Approx. Rs 21.00 / PieceGet Latest Price
Product Details:| Strength | 10 mg/ml |
| Packaging Size | 5 ml vial |
| Brand | Protamine |
| Indication | Heparin reversal |
| Route of Administration | IV slow |
| Usage | ICU |
| Storage Temperature | 2–8°C |
| Shelf Life | 24 months |
Healthy Inc offers Protamine Sulfate Injection IP, a critical heparin antagonist and life-saving reversal agent. Containing 10 mg of Protamine Sulfate per mL, this formulation is a clinical priority for neutralizing the anticoagulant effect of heparin, particularly after extracorporeal circulation (cardiac surgery or dialysis) or in cases of severe heparin-induced hemorrhage. As a specialized Indian export partner, we supply this essential rescue therapeutic to cardiac theaters, dialysis centers, and intensive care units in global pharmaceutical markets.
Clinical Precision: Acts through a simple acid-base reaction. Protamine (a strongly basic protein) forms a stable, inactive salt complex with Heparin (a strongly acidic polysaccharide), instantly neutralizing its anticoagulant properties.
Surgical Necessity: An absolute requirement for "bridge therapy" in surgery, allowing surgeons to rapidly restore normal coagulation once a patient is taken off a heart-lung machine or after vascular procedures.
Manufacturing Excellence: Produced in associated WHO-GMP certified sterile facilities. The solution is manufactured under strict aseptic conditions to ensure 100% sterility and a pyrogen-free profile, which is vital for rapid Intravenous (IV) bolus or infusion.
Climate Stability: Validated for Zone IVb (Hot/Humid) conditions; the formulation is stabilized to prevent protein denaturation and maintain potency across Africa, LATAM, and SEA markets.
Accepting B2B inquiries for contract manufacturing, bulk supply, and hospital distribution partnerships from our Mumbai export hub.
Available strengths and packaging? We supply Protamine Sulfate in the standard 50 mg / 5 mL (10 mg/mL) concentration, available in 5 mL ampoules or vials. Every batch undergoes rigorous biological assay testing and sterility validation to meet Indian Pharmacopoeia (IP) and international standards.
Support for tropical export? Yes. Our formulation is Zone IVb stability-tested. We utilize neutral USP Type I glass and specialized secondary packaging to ensure the protein remains stable during international transit to high-temperature regions.
Registration assistance provided? We provide complete Regulatory Technical Files (CTD) and Certificates of Analysis (COA) to facilitate local health authority approvals and government healthcare or cardiac-specialty tender participations.
Small-volume or mixed orders? We specialize in mixed-container consolidation, allowing you to combine Protamine Sulfate with other cardiac or emergency essentials (such as Heparin, Adrenaline, or Dopamine) in a single, cost-effective shipment.
Approx. Rs 260.60 / PieceGet Latest Price
Product Details:| Volume | 1 ml |
| Glass Type | Type I |
| Neck Type | Crimp Neck |
| Color | Clear |
| Sterility | Non Sterile |
| Vial Neck Size | 13 mm |
| Bottom Type | Flat Bottom |
| Graduation Mark | Without Mark |
| Pack Size | 25 pcs |
Healthy Inc offers RABALKEM, a high-efficiency Proton Pump Inhibitor (PPI) presented as a sterile lyophilized powder for injection. Containing 20 mg of Rabeprazole Sodium, this formulation is a clinical priority for the rapid treatment of severe acid-related disorders, including Zollinger-Ellison Syndrome, Gastroesophageal Reflux Disease (GERD) with erosive esophagitis, and the prevention of aspiration of acid during surgery. As a specialized Indian export partner, we supply this critical gastroenterology therapeutic to surgical wards and intensive care units in global pharmaceutical markets.
Clinical Precision: Acts by specifically inhibiting the H+/K+-ATPase enzyme system at the secretory surface of the gastric parietal cell. This "proton pump" blockade provides faster onset and more potent acid suppression compared to H2-receptor antagonists, making it ideal for acute gastric emergencies.
Manufacturing Excellence: Produced in associated WHO-GMP certified sterile facilities. The Lyophilized (freeze-dried) powder ensures maximum stability of the Rabeprazole molecule and allows for rapid, residue-free reconstitution for slow Intravenous (IV) injection or infusion.
Climate Stability: Validated for Zone IVb (Hot/Humid) conditions; the lyophilized form and vacuum-sealed USP Type I glass vials are engineered to maintain chemical integrity and potency across Africa, LATAM, and SEA markets.
Regulatory Support: Full technical documentation available, including CTD/eCTD Dossiers, to streamline the registration of essential GI therapeutics in your local territory.
Accepting B2B inquiries for contract manufacturing, bulk supply, and institutional distribution partnerships from our Mumbai export hub.
Available strengths and packaging? We supply RABALKEM in the standard 20 mg strength, presented in a vial with sterile Water for Injection. Every batch undergoes rigorous HPLC-based assay testing, sterility validation, and Bacterial Endotoxin Testing (BET) to meet international standards.
Support for tropical export? Yes. RABALKEM is Zone IVb stability-tested. We utilize neutral USP Type I glass vials and moisture-resistant secondary packaging to ensure the product remains stable and effective during international transit to high-temperature regions.
Registration assistance provided? We provide complete Regulatory Technical Files (CTD) and Certificates of Analysis (COA) to facilitate local health authority approvals and government healthcare or institutional tender participations.
Small-volume or mixed orders? We specialize in mixed-container consolidation, allowing you to combine RABALKEM with other critical care injectables (such as Pantoprazole, Ondansetron, or Tranexamic Acid) in a single, cost-effective shipment.
Direct sourcing? Products are sourced through Healthy Life Group’s associated WHO-GMP specialized manufacturing units, ensuring competitive direct-from-factory pricing and strict quality control oversight for essential gastro-care.
If you like, I can draft a high-authority LinkedIn post or a product profile for your e-commerce marketplace to help you promote RABALKEM to your international B2B buyers. Do you want me to do that?
Approx. Rs 47.48 / BottleGet Latest Price
Product Details:| Strength | 500 mg |
| Pack Type | Glass Vial |
| Form | Lyophilized Powder |
| Diluent | With Diluent |
| Route | IV |
| Brand | Pentothal |
| Pack Size | Single Vial |
| Storage | Store below 25°C |
| Shelf Life | 24 months |
Healthy Inc offers Thiopental Sodium for Injection, an ultra-short-acting thiobarbiturate and a cornerstone of intravenous anesthesia. As a pharmacist-led export firm, we supply this critical induction agent primarily for the rapid onset of unconsciousness in surgical settings. Produced in associated WHO-GMP certified sterile facilities, our Thiopental is engineered for high purity and rapid dissolution, managed directly from our Mumbai export hub.
GABAergic Modulation Mechanism: Thiopental works by binding to the $GABA_A$ receptor complex in the central nervous system. It increases the duration of chloride channel opening, enhancing the inhibitory effects of gamma-aminobutyric acid (GABA). This leads to immediate depression of the reticular activating system, resulting in hypnosis and anesthesia within 30–40 seconds of administration.
Clinical Criticality: Indicated for the induction of general anesthesia, the supplementation of regional anesthesia, and the control of convulsive states. In neurosurgery, it is also utilized for its neuroprotective properties, as it significantly reduces cerebral metabolic rate and intracranial pressure.
Pharmacokinetic Advantage: Due to its high lipid solubility, Thiopental rapidly crosses the blood-brain barrier. The quick recovery from a single bolus dose is not due to metabolism, but rather the rapid redistribution of the drug from the brain to leaner tissues (muscle and fat).
Manufacturing Excellence: Our product is supplied as a sterile, lyophilized yellow powder in an atmosphere of nitrogen. It contains anhydrous sodium carbonate as a buffer to ensure that the reconstituted solution remains strongly alkaline (pH 10.5–11.5), which is essential for maintaining the solubility of the barbiturate.
| Feature | Specification |
| Active Ingredient | Thiopental Sodium (with Sodium Carbonate) |
| Available Strengths | 500 mg / 1000 mg (1 gm) |
| Therapeutic Class | Ultra-short-acting Barbiturate / Anesthetic |
| Regulatory Status | WHO-GMP Certified Production |
| Primary Packaging | USP Type I Glass Vial (Sterile Powder) |
| Route of Admin. | Intravenous (IV) Only (Strictly avoid IA/SC) |
| Storage | Store below 30°C; Protect from Light |
As a pharmacist, you understand that Thiopental is a highly alkaline substance. The reconstituted solution is chemically incompatible with many other drugs (especially acidic ones like neuromuscular blockers), which can cause immediate precipitation. We provide clear technical labeling to ensure safety in the OR. Our logistics team optimizes shipments to Africa, LATAM, and SEA, utilizing moisture-proof secondary packaging to ensure the lyophilized powder remains free-flowing and stable in Zone IVb climates.
Approx. Rs 100 / BoxGet Latest Price
Product Details:| Strength | 500 mg |
| Pack Size | 10 capsules |
| Usage | Human |
| Brand | Almox |
| Packaging Type | Blister |
| Prescription | Prescription |
| Form | Capsule |
| Shelf Life | 24 months |
| Treatment | Bacterial Infection |
| Composition | Amoxicillin |
Healthy Inc offers the Flucloxacillin and Amoxicillin fixed-dose combination, a synergistic "broad-spectrum plus" antibiotic system. As a pharmacist-led firm, we recognize this combination (often referred to as Co-Fluampicil) as a strategic therapeutic for mixed infections where both Gram-positive Staphylococci and Gram-negative organisms are suspected. Managed from our Mumbai export hub, our formulation is produced in specialized WHO-GMP penicillin facilities.
Complementary Mechanism of Action:
Amoxicillin: A broad-spectrum amino-penicillin that targets a wide range of Gram-positive and Gram-negative bacteria by inhibiting cell wall synthesis. However, it is susceptible to degradation by beta-lactamase enzymes.
Flucloxacillin: A penicillinase-resistant penicillin. Its bulky side chain provides steric hindrance, protecting its own beta-lactam ring from hydrolysis by staphylococcal beta-lactamase.
The Clinical Synergy: In mixed infections, Flucloxacillin "covers" for the vulnerability of Amoxicillin against Staphylococcus aureus, while Amoxicillin extends the spectrum to include organisms like Streptococcus pyogenes and certain Gram-negative rods.
Clinical Indications:
Severe Skin and Soft Tissue Infections: Cellulitis and infected post-operative wounds where a mixed flora is suspected.
Upper Respiratory Tract Infections: Severe sore throats, sinusitis, and otitis media.
Septicemia: Initial empirical therapy for systemic infections before culture results are available.
Pharmacokinetic Profile: Both active ingredients are acid-stable and well-absorbed from the GI tract. They achieve peak plasma concentrations within 1–2 hours and exhibit excellent tissue penetration, particularly into skin, bone, and joint fluids.
| Feature | Specification |
| Active Ingredients | Amoxicillin (as Trihydrate) + Flucloxacillin (as Sodium) |
| Strength | 250 mg + 250 mg (Total 500 mg) |
| Therapeutic Class | Combination Penicillin Antibiotic |
| Regulatory Status | WHO-GMP Certified Production |
| Primary Packaging | Alu-Alu Blister / Alu-PVC Blister |
| Dosage Form | Hard Gelatin Capsule |
| Storage | Store below 30°C; Strictly Protect from Moisture |
As a pharmacist, you understand that Flucloxacillin Sodium is exceptionally hygroscopic. In a combination capsule, the moisture-attracting properties of Flucloxacillin can also lead to the degradation of the Amoxicillin component if not properly protected. We utilize Alu-Alu blister packaging as a mandatory standard for exports to Africa, LATAM, and SEA. This provides a 100% barrier against environmental humidity, ensuring the stability of the dual-penicillin matrix in Zone IVb climates throughout the transit from Mumbai.
Approx. Rs 51.57 / BoxGet Latest Price
Product Details:| Strength | 40 mg 75 mg |
| Packaging Size | 10 capsules |
| Packaging Type | Alu Alu |
| Brand | Cipla |
| Prescription | Prescription |
| Shelf Life | 24 months |
| Form | Capsule |
| Release Form | Sustained Release |
| Usage | Hospital |
Healthy Inc offers the Pantoprazole and Levosulpiride (Sustained Release) fixed-dose combination, a high-performance therapeutic for complex acid-peptic disorders. As a pharmacist, you recognize that while Domperidone is a standard prokinetic, Levosulpiride offers superior efficacy for patients with resistant GERD and functional dyspepsia due to its unique pro-cognitive and pro-motility properties. Managed through our Mumbai export hub, our formulation is produced in associated WHO-GMP certified facilities using advanced dual-pelletization technology.
Pharmacological SynergyThis combination provides a "dual-target" approach to gastrointestinal health:
Pantoprazole (40 mg): A substituted benzimidazole Proton Pump Inhibitor (PPI). It provides long-lasting suppression of gastric acid by irreversibly inhibiting the $H^+/K^+$-ATPase enzyme system. It is favored in clinical practice for its stable pharmacokinetic profile and low potential for drug-drug interactions (CYP2C19 metabolism).
Levosulpiride (75 mg SR): The levo-enantiomer of sulpiride, acting as a selective Dopamine ($D_2$) receptor antagonist. Unlike traditional prokinetics, Levosulpiride works at both peripheral and central levels to:
Increase the tone of the lower esophageal sphincter (LES).
Accelerate gastric emptying.
Exert a "pro-astenic" effect, reducing the visceral hypersensitivity often seen in functional dyspepsia.
Refractory GERD: For patients who remain symptomatic on standard PPI + Domperidone therapy.
Functional Dyspepsia: Management of bloating, early satiety, and upper abdominal pain.
Irritable Bowel Syndrome (IBS): Often used when IBS is accompanied by upper GI symptoms.
Diabetic Gastroparesis: Improving gastric transit time in diabetic patients.
| Feature | Specification |
| Active Ingredients | Pantoprazole (40 mg) + Levosulpiride (75 mg SR) |
| Therapeutic Class | Gastric Antisecretory + Atypical Prokinetic |
| Regulatory Status | WHO-GMP Certified Production |
| Primary Packaging | Alu-Alu Blister (Unit Dose) |
| Dosage Form | Hard Gelatin Capsule with Enteric Coated (EC) & SR Pellets |
| Storage | Store below 30°C; Protect from Heat & Moisture |
As a pharmacist, you understand that Pantoprazole is highly acid-labile and Levosulpiride is moisture-sensitive. For our exports to Africa, LATAM, and SEA, Healthy Inc utilizes Alu-Alu blister packaging as the mandatory standard. This provides a 100% hermetic seal, protecting the dual-pellet matrix from the high-humidity Zone IVb climates during the maritime journey from Mumbai.
Approx. Rs 9.38 / BottleGet Latest Price
Product Details:| Composition | Albendazole Ivermectin |
| Pack Size | 10 ml |
| Usage | Veterinary |
| Species | Cattle |
| Brand | Intas |
| Flavour | Unflavoured |
| Packaging Type | Bottle |
| Dosage Form | Oral Suspension |
| Shelf Life | 24 Month |
Healthy Inc offers the Albendazole and Ivermectin fixed-dose combination (FDC) suspension, a potent broad-spectrum anthelmintic therapy. As a pharmacist, you recognize this combination as the gold standard for "Mass Drug Administration" (MDA) programs, particularly in regions where Soil-Transmitted Helminths (STH) and Lymphatic Filariasis are co-endemic. Managed through our Mumbai export hub, our suspension is formulated for high palatability and uniform drug dispersion, ensuring accurate dosing for pediatric and adult populations.
We are offering ready stock of below top 30 Indian Brands & Generic Brand.
Bandicind-Plus, Zentel-Plus, Ivecop-AB, Noworm-Plus, Anthel-UP, Albura-I, Iver-A, Alminth-Plus, Bendex-Plus, Alben-I, Ivoral-Forte, Combantrin-Plus (Generic), Vermact-Plus, Albever, Iverm-AB, Albpure-I, Albstart-I, Albsift-I, Albford-I, Albnova-I, Albgard-I, Albzest-I, Alblap-I, Albspan-I, Albshine-I, Albrite-I, Albmed-I, Albsafe-I, Albplus-I, Albendazole-Ivermectin Healthy, Albendazole-Ivermectin Ajanta, Albendazole-Ivermectin Alkem, Albendazole-Ivermectin Sun, Albendazole-Ivermectin PMBJP.
Pharmacological Synergy: Dual-Mechanism Eradication
This combination utilizes two distinct biochemical pathways to ensure the complete immobilization and death of parasites:
Albendazole (200 mg per 5 ml): A benzimidazole derivative that acts by inhibiting tubulin polymerization. It binds to the $\beta$-tubulin of the parasite, preventing the formation of microtubules. This disrupts the parasite’s glucose uptake and ATP production, leading to energy depletion and death.
Ivermectin (1.5 mg per 5 ml): A semi-synthetic derivative of the avermectins. It binds selectively and with high affinity to glutamate-gated chloride channels in the invertebrate nerve and muscle cells. This leads to an increase in the permeability of the cell membrane to chloride ions, causing hyperpolarization of the nerve/muscle cell and resulting in the flaccid paralysis and death of the parasite.
Intestinal Nematodes: Effective against Roundworm (Ascaris lumbricoides), Whipworm (Trichuris trichiura), and Hookworm.
Lymphatic Filariasis: Used in global elimination programs to clear microfilariae from the bloodstream.
Strongyloidiasis: First-line treatment for intestinal infection caused by Strongyloides stercoralis.
Ectoparasitic Infestations: Adjunctive management for severe Scabies and Pediculosis (lice).
| Feature | Specification |
| Active Ingredients | Albendazole (200 mg) + Ivermectin (1.5 mg) per 5 ml |
| Therapeutic Class | Broad-Spectrum Anthelmintic |
| Regulatory Status | WHO-GMP Certified Production |
| Primary Packaging | Amber PET/Glass Bottles (10ml, 30ml, 60ml) |
| Formulation | Micronized Suspension (for enhanced bioavailability) |
| Storage | Store below 30°C; Shake well before use |
As a pharmacist, you understand that suspension stability is the primary technical challenge. In Zone IVb climates (high heat/humidity), improper formulation can lead to "caking" or irreversible sedimentation of the Albendazole particles.
Approx. Rs 100 / PieceGet Latest Price
Product Details:| Strength | 0.1% w/w |
| Pack Size | 5 g |
| Indication | Eczema |
| Form | Cream |
| Application Area | Body |
| Steroid Potency | Potent |
| Age Group | Adult |
| Prescription | Prescription |
| Pack Type | Tube |
Healthy Inc offers Betamethasone Valerate & Salicylic Acid Cream, a potent dermatological combination designed for the treatment of dry, scaly, and hyperkeratotic inflammatory skin conditions. As a pharmacist, you recognize that in conditions like chronic psoriasis or lichenified eczema, the skin develops a thick layer of dead keratin (the "skin barrier") that prevents standard corticosteroid creams from penetrating. This formulation solves that challenge: Salicylic Acid acts as a keratolytic agent to shed the scales, while Betamethasone Valerate provides the anti-inflammatory action. Managed through our Mumbai export hub, our cream is produced in WHO-GMP certified facilities with an optimized emulsion base.
We are offering ready stock of below top 30 Indian brands & Generic Brand.
Betnovate-S, Betasalic, Propysalic-NF, Tenovate-S, Diprobate-S, Sternon-SF, Saltopic, Biosalic, Betalic, Salis Tone, Betasalic-6, Misalic, Betagel-S, Lupiderm-S, Rovate-S, Salivate, Betafoam-S, Carebet-S, Dibederm-S, Betzees-S, Azonate-S, Prosalic-6, Betariv-S, Salisone-MF, Salisone-NU, Salisone-H, Betamethasone-Salicylic Healthy, Betamethasone-Salicylic Ajanta, Betamethasone-Salicylic Alkem, Betamethasone-Salicylic PMBJP.
Therapeutic Goal: To suppress inflammation, itching, and redness while simultaneously thinning the thickened skin layers to allow for better drug delivery.
Common Applications:
Psoriasis Vulgaris: Managing chronic plaques with silver scaling.
Chronic Atopic Dermatitis: Addressing lichenification (thickening of the skin due to chronic scratching).
Lichen Planus: Treating stubborn, inflammatory skin eruptions.
Hyperkeratotic Eczema: Managing dry, scaly eczema on the palms or soles.
Administration: Topical. Apply a thin layer to the affected area twice daily.
Pharmacist’s Note: As a professional, you should advise patients that this cream is highly potent. Use should be limited to the affected scaly areas only. Avoid application on the face, groin, or axilla where the skin is thin, as Salicylic Acid increases the penetration and systemic absorption of the corticosteroid, elevating the risk of skin atrophy or HPA-axis suppression.
Primary Classification: Potent Corticosteroid with Keratolytic.
Pharmacological Components:
Betamethasone Valerate: Mid-to-high potency (Class III) Corticosteroid.
Salicylic Acid: Keratolytic agent (Beta-Hydroxy Acid).
ATC Code: D07CC01.
| Feature | Specification |
|---|---|
| Active Ingredients | Betamethasone Valerate + Salicylic Acid |
| Common Strength | 0.1% w/w + 3.0% w/w (Standard Strength) |
| Regulatory Status | WHO-GMP Certified Production / BP / USP Compliant |
| Primary Packaging | 15g / 20g / 30g Lami-tubes with Tamper-evident seals |
| Base Type | Oil-in-Water (O/W) Vanishing Cream Base |
| Storage | Store below 30°C; Do not freeze |
Approx. Rs 10.32 / PieceGet Latest Price
Product Details:| Strength | 0.3% |
| Bottle Size | 10 ml |
| Dosage Form | Eye Drop |
| Use Case | Bacterial Infection |
| Patient Group | Adult |
| Prescription | Rx Only |
| Preservative | With Preservative |
| Pack Type | Plastic Bottle |
Healthy Inc offers this Antibiotic-Steroid Combination, a potent therapeutic solution for inflammatory ocular and otic infections. As a pharmacist, you recognize this formulation—often a suspension—as a dual-action treatment that addresses both the causative bacterial pathogen and the associated inflammatory response (pain, redness, and swelling). Managed through our Mumbai export hub, this product is manufactured in WHO-GMP certified sterile facilities.
We are offering ready stock of below top 30 Indian brands & Generic Brand.
Ciplox-D, Cifran-D, Zoxan-D, Ciprobid-D, Alcipro-D, Ceprolen-D, Joxin-D, Cifrox-D, Baycip-D, Cebran-D, Quintor-D, Stancipro-D, Ciprozen-D, Ciprowin-D, Ciprova-D, Ciflox-D, Cipron-D, Ciprodac-D, Cipro-HD, Cipro-MD, Cifro-D, Cipromac-D, Ciprocent-D, Cifrolex-D, Cipro-ODD, Ciprobest-D, Ciprofast-D, Ciprofloxacin-D PMBJP, Ciprofloxacin-D Healthy, Ciprofloxacin-D Ajanta
Product Usage & AdministrationTherapeutic Goal: To eradicate susceptible bacteria while suppressing the immune-mediated inflammatory damage to delicate ocular or otic tissues.
Common Applications:
Ophthalmic: Treating bacterial conjunctivitis or keratitis accompanied by significant inflammation or post-operative prophylaxis.
Otic (Ciprodex Type): Treating Acute Otitis Media in children with tympanostomy tubes or Acute Otitis Externa (Swimmer’s Ear).
Administration: * Eye: Typically 1–2 drops every 4–6 hours.
Ear: Typically 4 drops twice daily for 7 days.
Pharmacist’s Note: Because this is usually a suspension, counsel patients to shake the bottle well before each use. Advise them to avoid touching the dropper tip to any surface to maintain sterility. Limit use to the duration prescribed (usually 7–10 days) to prevent secondary fungal infections or steroid-induced ocular hypertension.
Primary Classification: Ophthalmic/Otic Antibacterial and Corticosteroid.
Pharmacological Components:
Ciprofloxacin (0.3% w/v): Second-generation Fluoroquinolone antibiotic.
Dexamethasone (0.1% w/v): Potent Glucocorticoid.
ATC Code: S01CA01 / S02CA06.
| Feature | Specification |
| Active Ingredients | Ciprofloxacin (0.3%) + Dexamethasone (0.1%) |
| Regulatory Status | WHO-GMP Certified Sterile Production / IP / BP / USP Grade |
| Primary Packaging | 5ml / 10ml LDPE Dropper Bottles |
| Formulation | Stabilized Ophthalmic/Otic Suspension |
| Stability | Optimized for long-term efficacy in Zone IVb (Tropical) climates |
| Storage | Store below 25°C; Do not freeze; Protect from light |
Approx. Rs 24.5 / PieceGet Latest Price
Product Details:| Brand | Refresh Tears |
| Pack Size | 3 ml |
| Composition | Carboxymethylcellulose |
| Concentration | 0.5 % w/v |
| Bottle Type | Plastic Bottle |
| Usage | Dry Eye |
| Shelf Life | 12 months |
| Sterility | Preserved |
| Prescription | Prescription |
| Bottle Color | White |
Healthy Inc offers this Antibiotic-Steroid Combination, a potent therapeutic for managing ocular inflammation associated with bacterial infection. As a pharmacist, you recognize this formulation as a "two-pronged" clinical approach: Chloramphenicol provides broad-spectrum bactericidal/bacteriostatic action, while Dexamethasone prevents the permanent tissue damage often caused by the body's own inflammatory response. Managed through our Mumbai export hub, these drops are produced in WHO-GMP certified sterile facilities.
We are offering ready stock of below top 30 Indian brands & Generic Brand.
Chloromycetin-D, Dexachlor, Opthocort, Chlorocol-D, Bellphenicol-D, Vanmycetin-D, Recetin-D, Aureomycin-D, Chlormet-D, Ocuchlor-D, Chloromax-D, C-Phenicol-D, Lycomycetin-D, Biomycetin-D, Renicol-D, Biosone-D, Chlor-PD, Chlorocort, Entomycetin-D, Paraxin-D, Mycetin-D, Chloroptic-D, Kloromex-D, Chlorgel-D, Chlorocet-D, Chloramphenicol-D PMBJP, Chloramphenicol-D Healthy, Chloramphenicol-D Ajanta, Chloramphenicol-D Cipla, Chloramphenicol-D Alkem
Product Usage & AdministrationTherapeutic Goal: To eradicate susceptible bacteria while simultaneously suppressing redness, swelling, and itching in the ocular tissues.
Common Indications:
Infectious Conjunctivitis: When accompanied by significant inflammatory symptoms.
Iritis & Uveitis: Managing internal inflammation where secondary bacterial infection is a risk.
Post-Operative Care: Preventing infection and reducing surgical inflammation after cataract or refractive surgery.
Administration: Ophthalmic. Instill 1 drop into the conjunctival sac 3 to 5 times daily. In acute cases, dosing may be increased under medical supervision.
Pharmacist’s Note: As a professional, you should counsel patients that this is a short-term therapy (usually 5–7 days). Prolonged use of topical steroids can lead to increased intraocular pressure (IOP) or secondary fungal infections. Advise them to avoid contact lenses during the entire treatment period.
Primary Classification: Ophthalmic Corticosteroid and Anti-infective.
Pharmacological Components:
Chloramphenicol (0.5% w/v): Broad-spectrum Antibiotic.
Dexamethasone Sodium Phosphate (0.1% w/v): Potent Glucocorticoid.
ATC Code: S01CA01.
| Feature | Specification |
| Active Ingredients | Chloramphenicol + Dexamethasone |
| Regulatory Status | WHO-GMP Certified Sterile Production / IP / BP / USP Grade |
| Primary Packaging | 5ml / 10ml LDPE Dropper Bottles |
| Preservative | Phenylmercuric Nitrate or Benzalkonium Chloride |
| Stability | Optimized for long-term efficacy in Zone IVb climates |
| Storage | Store between 2°C–8°C (Refrigerate); Protect from light |
Approx. Rs 76.85 / PieceGet Latest Price
Product Details:| Strength | 0.3% |
| Combination | Tobramycin Alone |
| Bottle Size | 5 ml |
| Use Case | Bacterial Infection |
| Dosage Form | Eye Drop |
| Patient Group | Adult |
| Preservative | With Preservative |
Healthy Inc offers Tobramycin & Dexamethasone Ophthalmic Suspension, a premier antibiotic-steroid combination. As a pharmacist, you recognize this formulation (often marketed as Tobradex) as a highly effective clinical solution for steroid-responsive inflammatory ocular conditions where a bacterial infection is present or where a high risk of infection exists. Managed through our Mumbai export hub, these drops are produced in WHO-GMP certified sterile facilities.
We are offering ready stock of below top 30 Indian brands & Generic Brand.
Tobra DM, Tobamex-D, Tobaren-D, Tobastar-D, Tobar-D, Tobasift-D, Tobacure-D, Tobasift-D, Eyebrex-D, Tobacin-D, Tobrex-D, Tobajay-D, Tobate-D, Tobalab-D, Tobawell-D, Tobasun-D, Tobacip-D, Tobamark-D, Tobabest-D, Tobafine-D, Tobapure-D, Tobamets-D, Tobabright-D, Tobashine-D, Tobaspan-D, Tobalap-D, Tobazest-D, Tobramycin-D PMBJP, Tobramycin-D Healthy, Tobramycin-D Ajanta
Therapeutic Goal: To provide a synergistic "one-two punch" by aggressively clearing bacterial pathogens while simultaneously suppressing the inflammatory cascade to prevent tissue damage.
Common Indications:
Post-Operative Prophylaxis: Preventing endophthalmitis and reducing surgical inflammation following cataract or refractive surgery.
Infectious Conjunctivitis & Keratitis: Treating severe "pink eye" or corneal inflammation involving susceptible bacteria.
Ocular Trauma: Managing inflammation and preventing secondary infection after chemical, radiation, or thermal burns.
Administration: Ophthalmic. Instill 1 or 2 drops into the conjunctival sac every 4 to 6 hours. During the initial 24 to 48 hours, the dosage may be increased to 1 or 2 drops every 2 hours.
Primary Classification: Ophthalmic Antibacterial and Corticosteroid.
Pharmacological Components:
Tobramycin (0.3% w/v): A potent Aminoglycoside antibiotic.
Dexamethasone (0.1% w/v): A high-potency Glucocorticoid.
ATC Code: S01CA01.
This combination addresses the root cause and the symptoms of ocular distress through two distinct pathways:
Tobramycin (The Protein Inhibitor):
It acts by binding to the 30S and 50S ribosomal subunits of the bacteria.
This leads to the disruption of protein synthesis, resulting in bactericidal action.
It is particularly effective against Gram-negative pathogens, including Pseudomonas aeruginosa, which are often resistant to other antibiotic classes.
| Feature | Specification |
| Active Ingredients | Tobramycin (0.3%) + Dexamethasone (0.1%) |
| Regulatory Status | WHO-GMP Certified Sterile Production / IP / BP / USP Grade |
| Primary Packaging | 5ml Opaque LDPE Dropper Bottles |
| Formulation | Micronized Ophthalmic Suspension |
| Stability | Optimized for integrity in Zone IVb (Tropical) climates |
| Storage | Store below 25°C; Do not freeze; Protect from light |
Approx. Rs 89.06 / PieceGet Latest Price
Product Details:| Composition | Xylometazoline |
| Strength | 0.05 % |
| Pack size | 10 ml |
| Brand | Nasivion |
| Age group | Infants |
| Usage | Nasal congestion |
| Form | Nasal drops |
| Prescription | Prescription |
| Packaging type | Dropper bottle |
| Shelf life | 12 months |
| Country of origin | India |
Healthy Inc offers Oxymetazoline Hydrochloride Nasal Solution, a highly effective long-acting topical decongestant. As a pharmacist, you recognize Oxymetazoline as a primary imidazoline derivative that provides rapid relief from nasal congestion by inducing powerful local vasoconstriction. Produced in WHO-GMP certified facilities, these drops are a core OTC and prescription staple in our Mumbai-based export operations.
We are offering ready stock of below top 30 Indian brands & Generic Brand.
Otrivin, Nasivion S, Xyloflo, Xylomet, Sinomet, Nosikind, Xylomist, Muconorm, Decon, Recofast, Zynose, Xynose, Rinostat, Nasoclear-X, Xylostar, Xylosun, Xylogard, Xylosift, Xylofine, Xylopure, Xylobest, Xylobrite, Xyloshine, Xylospan, Xylolap, Xylozest, Xylometazoline PMBJP, Xylometazoline Healthy, Xylometazoline Ajanta, Xylometazoline Sun
Therapeutic Goal: To provide rapid, long-lasting reduction of nasal airway resistance by shrinking swollen nasal membranes and reducing mucosal edema.
Common Indications:
Acute Rhinitis: Relief from the "stuffy nose" associated with the common cold or flu.
Allergic Rhinitis: Managing congestion caused by hay fever or other environmental allergies.
Sinusitis: Facilitating drainage of the sinuses by reducing ostial occlusion.
Therapeutic Category
Primary Classification: Topical Nasal Decongestant.
Pharmacological Class: Direct-acting Alpha-Adrenergic Agonist.
ATC Code: R01AA05.
| Feature | Specification |
| Active Ingredient | Oxymetazoline Hydrochloride BP / USP / IP |
| Concentrations | 0.05% (Adult) / 0.025% (Paediatric) |
| Regulatory Status | WHO-GMP Certified Production |
| Primary Packaging | 10ml / 15ml LDPE Dropper or Spray Bottles |
| Vehicle | Aqueous, isotonic solution buffered for nasal pH |
| Storage | Store below 30°C; Do not freeze |
Approx. Rs 154.69 / PieceGet Latest Price
Product Details:| Strength | 0.25 mg |
| Pack Size | 5 respules |
| Dosage Form | Respules |
| Composition | Budesonide |
| Brand | Budecort |
| Prescription Type | Prescription |
| Usage | Asthma |
| Age Group | Paediatric |
| Steroid Type | Inhaled Steroid |
Healthy Inc offers the Formoterol and Budesonide combination Metered Dose Inhaler (MDI). As a pharmacist and CEO, you recognize this as a fixed-dose combination (FDC) that represents the gold standard in modern asthma and COPD management. It combines a Long-Acting Beta-Agonist (LABA) with an Inhaled Corticosteroid (ICS) to provide both rapid symptom relief and long-term control. Produced in WHO-GMP certified facilities, these inhalers are a high-demand staple of our Mumbai-based export operations.
Product Usage & AdministrationTherapeutic Goal: To achieve simultaneous bronchodilation and anti-inflammatory control, reducing the frequency and severity of asthma attacks and COPD exacerbations.
Common Indications:
Asthma: For patients not adequately controlled on ICS alone or those whose disease severity warrants combination therapy.
COPD: For the maintenance treatment of airflow obstruction in patients with chronic bronchitis and emphysema.
Administration: Inhalation only.
Standard Dose: Usually 1 or 2 puffs twice daily (morning and evening).
SMART Therapy: In some clinical guidelines, this specific combination is used as both a maintenance and a "reliever" therapy due to Formoterol's rapid onset.
Primary Classification: Adrenergics in combination with corticosteroids.
Pharmacological Class: LABA + ICS.
ATC Code: R03AK07.
This combination is technically superior because it addresses the two primary components of airway disease:
Formoterol Fumarate (LABA):
Acts as a potent $\beta_2$-adrenoceptor agonist.
It triggers the relaxation of bronchial smooth muscle.
The Technical Edge: Unlike other LABAs (like Salmeterol), Formoterol has a rapid onset of action (1–3 minutes), similar to a rescue inhaler, while maintaining a long duration of effect (12 hours).
Budesonide (ICS):
A potent glucocorticoid with high local anti-inflammatory activity.
It reduces airway edema, mucus secretion, and the recruitment of inflammatory cells.
Synergy: Corticosteroids increase the expression of $\beta_2$-receptors, while $\beta_2$-agonists prime the glucocorticoid receptors for better activation.
| Feature | Specification |
| Active Ingredients | Formoterol Fumarate & Budesonide BP / USP / IP |
| Strengths (mcg) | 6/100, 6/200, 6/400 per puff |
| Regulatory Status | WHO-GMP Certified Production |
| Primary Packaging | 120 / 200 MDI doses in an Aluminum Canister |
| Propellant | HFA (Hydrofluoroalkane) – CFC-free |
| Storage | Store below 30°C; Protect from direct sunlight |
Approx. Rs 100 / BoxGet Latest Price
Product Details:| Strength | 20 mg |
| Packaging Size | 7 Sachets |
| Brand | Apcalis-SX |
| Flavor | Assorted |
| Manufacturer | Ajanta Pharma |
| Form | Oral Jelly |
| Composition | Tadalafil |
Healthy Inc offers Tadalafil & Dapoxetine Oral Jelly, a potent dual-action formulation designed to address both Erectile Dysfunction (ED) and Premature Ejaculation (PE). As a pharmacist and CEO of a pharmaceutical manufacturing and trading firm, you recognize that this "combination therapy" is highly sought after in the B2B sector for its synergistic effect and rapid absorption profile. Produced in WHO-GMP certified facilities, this oral jelly is a high-velocity item for your e-commerce marketplace and global pharmaceutical exports from our Mumbai hub.
Product Usage & Clinical ApplicationsTherapeutic Goal: To simultaneously improve erectile quality and increase the time to ejaculation.
Common Indications:
Dual Dysfunction: Patients experiencing both ED and PE concurrently.
Performance Anxiety: Managing the physiological symptoms of sexual dysfunction related to psychological stress.
Administration: Oral. The jelly is squeezed from the sachet directly into the mouth.
Timing: Consume approximately 30 to 60 minutes before sexual activity.
Absorption: The jelly form allows for faster sublingual and mucosal absorption compared to traditional tablets, often leading to a quicker onset of action.
Primary Classification: Urological / Sex Stimulants.
Pharmacological Class:
Tadalafil: Phosphodiesterase type 5 (PDE5) inhibitor.
Dapoxetine: Selective Serotonin Reuptake Inhibitor (SSRI).
ATC Code: G04BE30 (Combinations).
This formulation works through two distinct biochemical pathways to restore sexual function:
Hemodynamic Action (Tadalafil): Tadalafil inhibits the PDE5 enzyme, preventing the degradation of cyclic Guanosine Monophosphate (cGMP) in the smooth muscles of the corpus cavernosum. This leads to prolonged vasodilation and increased blood flow to the penis.
Neurochemical Action (Dapoxetine): Dapoxetine inhibits the serotonin transporter, increasing serotonin's action at the post-synaptic cleft. By delaying the neuronal signal associated with ejaculation, it provides greater control over the ejaculatory reflex.
| Feature | Specification |
| Active Ingredients | Tadalafil ($20\text{ mg}$) + Dapoxetine ($60\text{ mg}$) |
| Dosage Form | Oral Jelly (Semi-solid Suspension) |
| Regulatory Status | WHO-GMP Certified Production |
| Primary Packaging | $5\text{g}$ Multi-laminate foil sachets |
| Flavors | Orange, Strawberry, Pineapple, Mint, or Mixed Fruit |
| Stability | Optimized for shelf-life in Zone IVb (Tropical) climates |
| Storage | Store below $30^\circ\text{C}$; Do not freeze |
Approx. Rs 100 / BoxGet Latest Price
Product Details:| Strength | 20 mg |
| Packaging Size | 7 Sachets |
| Brand | Apcalis-SX |
| Flavor | Assorted |
| Manufacturer | Ajanta Pharma |
| Form | Oral Jelly |
| Composition | Tadalafil |
| Prescription/Non prescription | Prescription |
Healthy Inc offers Tadalafil Oral Jelly, a rapid-acting treatment for Erectile Dysfunction (ED). As a pharmacist and CEO, you recognize Tadalafil as a "long-acting" PDE5 inhibitor, often referred to as the "weekend pill" due to its extended half-life. The jelly formulation is specifically engineered for patients who have difficulty swallowing tablets (dysphagia) or those seeking a faster onset of action through mucosal absorption. Produced in WHO-GMP certified facilities, this product is a high-demand item for your e-commerce marketplace and global pharmaceutical exports from our Mumbai hub.
Product Usage & Clinical ApplicationsTherapeutic Goal: To improve erectile function by increasing blood flow to the penis during sexual stimulation.
Common Indications:
Erectile Dysfunction (ED): Managing the inability to achieve or maintain a penile erection sufficient for satisfactory sexual performance.
Benign Prostatic Hyperplasia (BPH): Occasionally used to treat the signs and symptoms of an enlarged prostate.
Administration: Oral. Squeeze the contents of the sachet directly into the mouth or onto a spoon.
Timing: Consume approximately 15 to 30 minutes before anticipated sexual activity.
Duration: The effects can last for up to 36 hours, providing a significantly wider window of opportunity compared to Sildenafil.
Primary Classification: Urological / Drugs used in Erectile Dysfunction.
Pharmacological Class: Phosphodiesterase type 5 (PDE5) inhibitor.
ATC Code: G04BE08.
Tadalafil works by modulating the natural chemical response to sexual arousal:
Nitric Oxide Release: Sexual stimulation triggers the local release of nitric oxide in the corpus cavernosum.
cGMP Accumulation: Nitric oxide activates the enzyme guanylate cyclase, which increases levels of cyclic Guanosine Monophosphate (cGMP).
PDE5 Inhibition: Tadalafil selectively inhibits the PDE5 enzyme, which is responsible for breaking down cGMP.
Smooth Muscle Relaxation: By maintaining high cGMP levels, Tadalafil ensures sustained smooth muscle relaxation and increased blood inflow, resulting in an erection.
| Feature | Specification |
| Active Ingredient | Tadalafil USP / BP / IP |
| Concentration | $20\text{ mg}$ per sachet |
| Dosage Form | Oral Jelly (Semi-solid Suspension) |
| Regulatory Status | WHO-GMP Certified Production |
| Primary Packaging | $5\text{g}$ Multi-laminate moisture-proof sachets |
| Flavors | Orange, Strawberry, Pineapple, Mint, or Mixed Fruit |
| Storage | Store below $30^\circ\text{C}$; Do not freeze |
Approx. Rs 33.70 / BoxGet Latest Price
Product Details:| Strength | 100 mg/ml |
| Pack Size | 1 ml |
| Pack Type | Ampoule |
| Route | IV |
| Grade | IP |
| Sugar Free | Yes |
| Form | Injection |
| Prescription | Prescription |
| Shelf Life | 12 months |
Healthy Inc offers LIGOCARE-A, a high-precision Local Anesthetic with Vasoconstrictor. Combining Lignocaine Hydrochloride for rapid-onset nerve blockade and Adrenaline (Epinephrine) for localized vasoconstriction, LIGOCARE-A is a clinical priority for procedures requiring extended anesthesia and minimized localized bleeding. It is a frontline therapeutic for Dental Procedures, Minor Surgical Infiltrations, and Peripheral Nerve Blocks. As a specialized Indian export partner, we supply this essential anesthetic to dental clinics, trauma centers, and surgical units in global pharmaceutical markets.
Extended Duration: The addition of Adrenaline at a 1:80,000 ratio reduces systemic absorption of Lignocaine, significantly prolonging the anesthetic effect and providing a clearer surgical field (hemostasis).
Manufacturing: Produced in associated WHO-GMP certified sterile facilities, ensuring 100% sterility, precise pH balancing, and exact dilution of the vasoconstrictor component.
Climate Stability: Validated for Zone IVb (Hot/Humid) conditions; our formulation is stabilized to prevent the rapid oxidation of Adrenaline, ensuring potency across Africa, LATAM, and SEA markets.
Regulatory Support: Full technical documentation available, including CTD/eCTD Dossiers, to streamline the registration of essential anesthetic injectables.
Accepting B2B inquiries for contract manufacturing, bulk supply, and global distribution partnerships from our Mumbai export hub.
Available packaging and quality? We supply LIGOCARE-A in 30 ml and 50 ml multi-dose vials, as well as 2 ml ampoules. Every batch undergoes rigorous HPLC-based assay testing for both active ingredients and sterility validation to meet international pharmacopoeia standards.
Support for tropical export? Yes. Adrenaline is highly sensitive to light and heat; however, LIGOCARE-A is Zone IVb stability-tested. We utilize neutral USP Type I amber glass and specialized export-grade secondary packaging to protect the molecule from oxidation during international transit.
Registration assistance provided? We provide complete Regulatory Technical Files (CTD) and Certificates of Analysis (COA) to facilitate local health authority approvals and government dental or surgical tender participations in your specific territory.
Small-volume or mixed orders? We specialize in mixed-container consolidation, allowing you to combine LIGOCARE-A with other surgical essentials (such as plain Lignocaine, Bupivacaine, or Ketorolac) in a single, cost-effective shipment.
Direct sourcing? Products are sourced through Healthy Life Group’s associated WHO-GMP manufacturing units, ensuring competitive direct-from-factory pricing and strict quality control oversight for essential pain management and anesthetic therapies.
Approx. Rs 413.43 / VialGet Latest Price
Product Details:| Brand | Meronem |
| Form | Vial |
| Composition | Meropenem |
| Route of Administration | IV |
| Packaging Size | 1 vial |
| Injection Type | Lyophilized powder |
| Pharmacopoeia Standard | IP |
| Usage | Human |
| Strength | 1 g |
Healthy Inc offers MEROBAX 250 mg, a specialized dosage of the ultra-broad-spectrum Carbapenem Antibiotic, Meropenem. This intermediate strength is a clinical priority for precise dose titration in Pediatric Patients, as well as for adult patients with Renal Impairment (CrCl 25–50 ml/min) where a reduced dose is required. It is a frontline therapeutic for Nosocomial Pneumonia, Complicated Urinary Tract Infections (cUTI), and Neonatal Septicemia. As a specialized Indian export partner, we supply this critical anti-infective to neonatal units and specialized clinics in global pharmaceutical markets.
Dosing Precision: Provides an ideal middle-ground concentration, reducing medication waste and the risk of contamination associated with dividing larger 500 mg or 1 g vials for low-weight or renal patients.
Manufacturing: Produced in associated WHO-GMP certified sterile facilities specialized in Lyophilization, ensuring 100% sterility, high molecular purity, and rapid reconstitution for Intravenous (IV) administration.
Climate Stability: Validated for Zone IVb (Hot/Humid) conditions; the lyophilized powder form ensures the stability of the Carbapenem molecule across the tropical climates of Africa, LATAM, and SEA markets.
Regulatory Support: Full technical documentation available, including CTD/eCTD Dossiers, to facilitate the registration of specialized anti-infectives.
Accepting B2B inquiries for contract manufacturing, bulk supply, and global distribution partnerships from our Mumbai export hub.
Available strengths and quality? We supply MEROBAX in 250 mg, 125 mg, 500 mg, and 1000 mg vials. Every batch undergoes rigorous HPLC-based assay testing, sterility validation, and Bacterial Endotoxin Testing (BET) to meet USP and international pharmacopoeia standards.
Support for tropical export? Yes. MEROBAX 250 mg is Zone IVb stability-tested. We utilize neutral USP Type I glass vials and moisture-resistant secondary packaging to ensure product integrity during international transit to high-temperature regions.
Registration assistance provided? We provide complete Regulatory Technical Files (CTD) and Certificates of Analysis (COA) to facilitate local health authority approvals and specialized hospital tender participations.
Small-volume or mixed orders? We specialize in mixed-container consolidation, allowing you to combine MEROBAX 250 mg with other critical care essentials (such as Amikacin, Ceftriaxone, or specialized IV fluids) in a single, cost-effective shipment.
Direct sourcing? Products are sourced through Healthy Life Group’s associated WHO-GMP specialized manufacturing units, ensuring competitive direct-from-factory pricing and strict quality control oversight for high-end antibiotic therapies.
Approx. Rs 52.00 / PieceGet Latest Price
Product Details:| Strength | 100 mcg/ml |
| Pack Size | 1 ml |
| Pack Type | Ampoule |
| Route | IM |
| With B Complex | Yes |
| Grade | IP |
| Form | Injection |
| Prescription | Prescription |
| Shelf Life | 18 months |
Healthy Inc offers Cyanocobalamin Injection, a high-purity, synthetic form of Vitamin $B_{12}$. Containing 500 mcg of sterile Cyanocobalamin per mL, this formulation is a clinical priority for the rapid correction of severe vitamin $B_{12}$ deficiencies and the management of various hematological and neurological disorders. As a specialized Indian export partner, we supply this essential micronutrient to hospitals, geriatric centers, and wellness clinics globally.
Hematological Precision: Cyanocobalamin is essential for DNA synthesis and the maturation of red blood cells. It is the gold standard for treating Pernicious Anemia (where oral absorption is compromised due to lack of intrinsic factor) and other macrocytic/megaloblastic anemias.
Neurological Support: Vitamin $B_{12}$ plays a critical role in the maintenance of the myelin sheath that surrounds nerves. Injectable 500 mcg doses are utilized to treat and prevent peripheral neuropathies and subacute combined degeneration of the spinal cord.
Superior Bioavailability: While oral $B_{12}$ depends heavily on gastric pH and intestinal health, the injectable format provides 100% molecular bioavailability, ensuring rapid replenishment of hepatic $B_{12}$ stores.
Manufacturing Excellence: Produced in associated WHO-GMP certified sterile facilities. The solution is formulated with precise pH control and protected from light to prevent the photodegradation of the cobalamin molecule.
Climate-Adaptive Stability: Validated for Zone IVb (Hot/Humid) conditions. Encapsulated in USP Type I amber glass ampoules or vials to maintain 100% sterility and chemical stability during international transit to Africa, LATAM, and SEA markets.
Accepting B2B inquiries for high-volume supply, institutional healthcare tenders, and global distribution from our Mumbai export hub.
B2B Technical Specifications| Feature | Specification |
| Active Ingredient | Cyanocobalamin (Vitamin $B_{12}$) |
| Strength | 500 mcg / mL |
| Therapeutic Class | Vitamin / Hematopoietic Agent |
| Regulatory Status | WHO-GMP Certified Production |
| Primary Packaging | USP Type I Amber Glass Ampoule |
| Storage | Store below 30°C; Protect from Light |
Logistics & Export Optimization
As a pharmacist-led firm, we understand that Cyanocobalamin is highly sensitive to light. We utilize specialized light-shielding secondary packaging and reinforced cartons to ensure the product reaches your clinical facility without any molecular breakdown. Our logistics team optimizes shipments from Mumbai to ensure cost-effective delivery for regional distributors.
Approx. Rs 1,579.69 / PieceGet Latest Price
Product Details:| Strength | 300 µg |
| Dose Volume | 2 ml |
| Indication | Antenatal |
| Source | Human |
| Presentation | PFS |
| Route | IM |
| Storage Temp | 2–8°C |
Healthy Inc offers Rhoclone, a high-precision, sterile solution of Anti-D (Rh) Immunoglobulin. As a specialized Indian export partner, we supply this critical biological therapeutic for the prevention of Rh isoimmunization. Produced in associated WHO-GMP certified facilities using advanced monoclonal or plasma-derived technology, Rhoclone is a life-saving essential in obstetric care globally, managed from our Mumbai export hub.
Mechanism of Immunosuppression: Rhoclone works by providing passive immunity. It contains antibodies against the Rh0(D) antigen found on red blood cells. When administered to an Rh-negative mother carrying an Rh-positive fetus, the Anti-D antibodies neutralize any fetal Rh-positive cells that enter the maternal circulation, preventing the mother’s immune system from becoming sensitized and producing its own antibodies.
Clinical Criticality: Indicated for the prevention of Hemolytic Disease of the Newborn (HDN). It is administered to Rh-negative women after the birth of an Rh-positive infant, or following events where feto-maternal hemorrhage may occur (miscarriage, abortion, ectopic pregnancy, or abdominal trauma).
Hematological Utility: Also utilized in the treatment of Immune Thrombocytopenic Purpura (ITP) in Rh-positive, non-splenectomized patients to increase platelet counts by interfering with the clearance of antibody-coated platelets.
Manufacturing Excellence: Our product undergoes rigorous viral inactivation and ultra-filtration processes. It is available in Pre-Filled Syringes (PFS) for immediate clinical use, ensuring dose accuracy and maintaining a sterile closed-loop system during Intramuscular (IM) or Intravenous (IV) administration.
| Feature | Specification |
| Active Ingredient | Anti-D (Rh) Immunoglobulin |
| Available Strengths | 150 mcg (750 IU) / 300 mcg (1500 IU) |
| Therapeutic Class | Immunomodulator / Biological Product |
| Regulatory Status | WHO-GMP Certified / Plasma Master File Compliance |
| Primary Packaging | Pre-Filled Syringe (PFS) / USP Type I Glass Vial |
| Storage | Cold Chain Required: 2°C to 8°C |
As a pharmacist, you are well aware that Anti-D Immunoglobulin is a highly heat-labile biological. Exposure to ambient temperatures for even short periods can cause protein denaturation, rendering the injection ineffective. We utilize validated cold-chain shipping solutions, including vacuum-insulated panels and electronic temperature loggers, for all shipments to Africa, LATAM, and SEA. This ensures that the "Fridge-to-Clinic" integrity is maintained throughout the transit from Mumbai.
Approx. Rs 1,371.57 / BottleGet Latest Price
Product Details:| Strength | 20 mg |
| Brand | Temonat |
| Capsules per Pack | 5 Capsules |
| Pack Type | Bottle |
| Form | Capsule |
| Usage | Brain Tumor |
| Prescription Type | Prescription |
Healthy Inc offers Temozolomide, a second-generation oral alkylating agent and the standard-of-care for high-grade gliomas. As a pharmacist, you recognize that Temozolomide is a prodrug specifically designed to cross the Blood-Brain Barrier (BBB), making it one of the few effective oral treatments for CNS malignancies. Managed through our Mumbai export hub, our formulation is produced in specialized WHO-GMP cytotoxic manufacturing units under strict containment protocols.
Pharmacological ProfileMechanism of Action (DNA Alkylation): Temozolomide is stable at acidic pH but undergoes rapid non-enzymatic conversion to its active metabolite, MTIC (monomethyl triazenoimidazole carboxamide), at physiological pH ($>7.0$). MTIC methylates DNA, primarily at the $O^6$ and $N^7$ positions of guanine. This methylation causes DNA mismatch, which the cell's repair machinery cannot fix, leading to DNA strand breaks and subsequent apoptosis (cell death).
Clinical Efficacy (The Stupp Protocol):
Glioblastoma Multiforme (GBM): Used concomitantly with radiotherapy and then as maintenance therapy.
Anaplastic Astrocytoma: For patients who have experienced relapse after nitrosourea and procarbazine therapy.
The MGMT Factor: As a pharmacist, you know that the clinical response often depends on the MGMT (O6-methylguanine-DNA methyltransferase) gene promoter methylation status. Patients with a "silenced" (methylated) MGMT gene typically show a significantly better response to Temozolomide because their cells cannot repair the DNA damage caused by the drug.
| Feature | Specification |
| Active Ingredient | Temozolomide |
| Available Strengths | 5 mg, 20 mg, 100 mg, 250 mg |
| Therapeutic Class | Antineoplastic (Alkylating Agent) |
| Regulatory Status | WHO-GMP Cytotoxic Certified |
| Primary Packaging | Opaque HDPE Bottles / Child-Resistant Blisters |
| Dosage Form | Hard Gelatin Capsule |
| Storage | Store below 25°C; Protect from Moisture & Light |
As a pharmacist, you understand that Temozolomide is a hazardous cytotoxic drug. It requires specialized handling to prevent accidental exposure to personnel and environmental contamination. The capsules must remain intact; they should never be opened or crushed.
Approx. Rs 100 / PieceGet Latest Price
Product Details:| Strength | 1% w/w |
| Pack Size | 10 g |
| Prescription | OTC |
| Brand | Calamine |
| Form | Cream |
| Composition | Tolnaftate 1% |
| Usage Area | Feet |
| Packing Type | Tube |
| Shelf Life | 24 months |
Healthy Inc offers Tolnaftate Cream, a synthetic Thiocarbamate Antifungal agent that has been a mainstay in dermatological care for decades. As a pharmacist, you recognize Tolnaftate as a unique alternative to allylamines and azoles, particularly effective for the treatment and prevention of superficial fungal infections. Managed through our Mumbai export hub, our cream is produced in WHO-GMP certified facilities, providing a reliable and safe solution for retail and institutional pharmaceutical markets.
We are offering ready stock of below top 30 Indian brands & Generic Brand.
Tinaderm, Tolnaderm, Toloder, Tolmicen, Tonal, Tolnapure, Tolnastart, Tolnasift, Tolnaford, Tolnanova, Tolnagard, Tolnazest, Tolnalap, Tolnaspan, Tolnashine, Tolnabrite, Tolnamed, Tolnasafe, Tolnaplus, Tolnahealth, Tolnabest, Tolnacare, Tolnafast, Tolnafine, Tolnazen, Tolnaftate Healthy, Tolnaftate Ajanta, Tolnaftate Sun, Tolnaftate Alkem, Tolnaftate PMBJP.
Product Usage & AdministrationTherapeutic Goal: To stop the growth of fungi and prevent the recurrence of infections in the stratum corneum.
Common Applications:
Tinea Pedis (Athlete's Foot): Effective for both interdigital and "moccasin-type" infections.
Tinea Cruris (Jock Itch): Relieving localized itching and burning in skin folds.
Tinea Corporis (Ringworm): Managing circular lesions on the body.
Preventive Use: When applied daily, it helps prevent the recurrence of athlete's foot in high-risk environments.
Administration: Topical. Thoroughly clean and dry the affected area. Apply a thin layer twice daily (morning and night).
+2
Pharmacist’s Note: As a professional, you should counsel patients to continue treatment for at least 2 weeks after symptoms disappear to ensure complete eradication. Tolnaftate is often preferred for long-term prophylaxis because of its low irritation profile compared to some azoles.
| Feature | Specification |
|---|---|
| Active Ingredient | Tolnaftate USP / BP / IP |
| Concentration | 1% w/w |
| Regulatory Status | WHO-GMP Certified Production |
| Primary Packaging | 15g / 30g Lami-tubes |
| Base Type | Odorless, non-greasy Vanishing Cream |
| Stability | Optimized for consistent performance in Zone IVb climates |
| Storage | Store at 15°C–30°C; Do not freeze |
Approx. Rs 211 / PieceGet Latest Price
Product Details:| Strength | 50 mcg |
| Pack Size | 80 doses |
| Dosage Form | MDI Inhaler |
| Composition | Beclomethasone |
| Brand | Beclate |
| Prescription Type | Prescription |
| Usage | Asthma |
| Age Group | Paediatric |
| Steroid Type | Inhaled Steroid |
Healthy Inc offers Beclomethasone Dipropionate (BDP) in a Metered Dose Inhaler (MDI) format. As a pharmacist and CEO, you recognize this as a foundational Inhaled Corticosteroid (ICS) for the long-term, maintenance treatment of chronic asthma. Unlike rescue inhalers, Beclomethasone targets the underlying pathology of the disease—chronic airway inflammation. Produced in WHO-GMP certified facilities, these inhalers are a high-volume export staple from our Mumbai hub.
Product Usage & AdministrationTherapeutic Goal: To maintain long-term control of asthma symptoms and prevent acute exacerbations.
Common Indications:
Prophylactic Management: For patients who require regular treatment to prevent bronchospasm.
COPD: Often used as an adjunct in patients with severe symptoms or frequent exacerbations.
Administration: Inhalation only.
Standard Dose: Usually 1 to 2 puffs (pMDI) twice daily.
Tapering: Once control is achieved, the dose should be titrated to the lowest effective level.
Pharmacist’s Note: This is the most vital counseling point: "Rinse and Spit." Advise patients to rinse their mouth with water and spit it out after every use to prevent Oropharyngeal Candidiasis (thrush). Remind them that this is a preventer, not a reliever; it will not work during an active asthma attack.
Primary Classification: Inhaled Corticosteroid (ICS).
Pharmacological Class: Glucocorticoid.
ATC Code: R03BA01.
| Feature | Specification |
| Active Ingredient | Beclomethasone Dipropionate BP / USP / IP |
| Strength | 100 mcg / 200 mcg per puff |
| Regulatory Status | WHO-GMP Certified Production |
| Primary Packaging | 200 MDI doses in an Aluminum Canister with Actuator |
| Propellant | HFA (Hydrofluoroalkane) – CFC-free and Ozone-friendly |
| Storage | Store below 30°C; Protect from direct sunlight |
Product Price :Get Latest Price
Product Details:| Strength | 4 mg |
| Brand | Zoltero |
| Manufacturer | Natco Pharma Ltd |
| Treatment | Hypercalcemia |
| Pharmacopoeia Standard | IP |
| Packaging Type | Vial |
| Storage Temperature | 23-25 degree c |
| Shelf Life | 24 months |
| Volume | 100 ml |
| Composition | Zoledronic Acid |
Healthy Inc offers NORADNALIN 4, a critical-care Vasopressor and Sympathomimetic agent essential for hemodynamic stabilization. Containing Norepinephrine Bitartrate (equivalent to 4 mg of Norepinephrine base in 2 mL), this formulation is a clinical priority for the restoration of blood pressure in acute hypotensive states. It is the gold-standard frontline therapeutic for Septic Shock, Cardiogenic Shock, and post-operative Vasoplegic Syndrome. As a specialized Indian export partner, we supply this life-saving injectable to Intensive Care Units (ICUs), emergency departments, and cardiac surgery centers in global pharmaceutical markets.
Hemodynamic Precision: Primarily acts on alpha-adrenergic receptors to induce potent peripheral vasoconstriction, increasing systemic vascular resistance and mean arterial pressure (MAP) while providing modest beta-1 stimulation for inotropic support.
Manufacturing Excellence: Produced in associated WHO-GMP certified sterile facilities. The solution is manufactured under an inert nitrogen atmosphere to prevent oxidation, ensuring 100% sterility and high molecular purity for Intravenous (IV) infusion.
Climate Stability: Validated for Zone IVb (Hot/Humid) conditions. Because Norepinephrine is highly sensitive to oxygen and light, NORADNALIN 4 is stabilized with specialized buffers and protected in amber glass to ensure potency across Africa, LATAM, and SEA markets.
Regulatory Support: Full technical documentation available, including CTD/eCTD Dossiers, to streamline the registration of essential emergency-medicine therapeutics.
Accepting B2B inquiries for contract manufacturing, bulk supply, and global distribution partnerships from our Mumbai export hub.
Available strengths and packaging? We supply NORADNALIN in the 4 mg / 2 mL (2 mg/mL) concentration, which is the international standard for dilution in IV bags (D5W or Normal Saline). Every batch undergoes rigorous HPLC-based assay testing, sterility validation, and Bacterial Endotoxin Testing (BET) to meet USP/BP standards.
Support for tropical export? Yes. Norepinephrine is prone to rapid degradation if exposed to light or air. NORADNALIN 4 is Zone IVb stability-tested, and we utilize neutral USP Type I amber glass ampoules and specialized moisture-resistant secondary packaging to ensure product integrity during international transit.
Registration assistance provided? We provide complete Regulatory Technical Files (CTD) and Certificates of Analysis (COA) to facilitate local health authority approvals and critical-care government tender participations in your specific territory.
Small-volume or mixed orders? We specialize in mixed-container consolidation, allowing you to combine NORADNALIN 4 with other emergency cardiac injectables (such as Dopamine, Dobutamine, or Atropine) in a single, cost-effective shipment.
Direct sourcing? Products are sourced through Healthy Life Group’s associated WHO-GMP manufacturing units, ensuring competitive direct-from-factory pricing and strict quality control oversight for essential life-saving vasopressor therapies.
Product Price :Get Latest Price
Product Details:| Strength | 100 mg |
| Physical Form | Oil-Based Solution |
| Route of Administration | Intramuscular |
| Brand | Masteron |
| Treatment | Breast Cancer |
| Manufacturer | Generic Manufacturer |
| Packaging Size | 10 x 10 |
| Storage Condition | 20-25 degree c |
| Shelf Life | 24 months |
| Container Type | Vial |
| Composition | Drostanolone Propionate |
| Dosage Form | Injection |
Healthy Inc offers HITCORT-100, a high-velocity Glucocorticoid and essential corticosteroid for emergency medicine. Containing Hydrocortisone Sodium Succinate, it is designed for rapid systemic effect where oral therapy is not possible or immediate intervention is life-saving. It is a clinical priority for the management of Status Asthmaticus, Anaphylactic Reactions, Adrenal Crisis, and severe Inflammatory Conditions. As a specialized Indian export partner, we supply this critical care injectable to emergency departments and trauma centers in global pharmaceutical markets.
Clinical Utility: Acts as a potent anti-inflammatory and immunosuppressant. It is the gold standard for restoring hemodynamic stability in patients with acute adrenal insufficiency and managing life-threatening allergic emergencies.
Manufacturing: Produced in associated WHO-GMP certified sterile facilities specialized in lyophilization (freeze-drying), ensuring 100% sterility, high molecular purity, and instant reconstitution.
Climate Stability: Validated for Zone IVb (Hot/Humid) conditions; the lyophilized form provides superior stability compared to liquid formulations, ensuring potency across Africa, LATAM, and SEA markets.
Regulatory Support: Full technical documentation available, including CTD/eCTD Dossiers, to streamline the registration process for essential emergency therapeutics.
Accepting B2B inquiries for contract manufacturing, bulk supply, and global distribution partnerships from our Mumbai export hub.
Available strengths and quality? We supply HITCORT-100 as a vial containing 100 mg of Hydrocortisone Sodium Succinate as a sterile cake/powder. Every batch undergoes rigorous HPLC-based assay testing, sterility validation, and Bacterial Endotoxin Testing (BET) to meet Indian Pharmacopoeia (IP) and international standards.
Support for tropical export? Yes. HITCORT-100 is Zone IVb stability-tested. The lyophilized powder is highly resistant to thermal degradation. We utilize neutral USP Type I glass vials and moisture-resistant secondary packaging to ensure integrity during international transit to high-temperature regions.
Registration assistance provided? We provide complete Regulatory Technical Files (CTD) and Certificates of Analysis (COA) to facilitate local health authority approvals and government hospital tender participations in your specific territory.
Small-volume or mixed orders? We specialize in mixed-container consolidation, allowing you to combine HITCORT-100 with other emergency injectables (such as Adrenaline, Atropine, or Dexamethasone) and IV fluids in a single, cost-effective shipment.
Direct sourcing? Products are sourced through Healthy Life Group’s associated WHO-GMP manufacturing units, ensuring competitive direct-from-factory pricing and strict quality control oversight for essential corticosteroid therapies.
Approx. Rs 435.00 / BottleGet Latest Price
Product Details:| Strength | 5 mg |
| Brand | Lenalid |
| Capsules per Pack | 30 Capsules |
| Usage | Multiple Myeloma |
| Form | Capsule |
| Pack Type | Bottle |
Healthy Inc offers Lenalidomide Capsules, a potent immunomodulatory imide drug (IMiD) and a derivative of thalidomide. As a pharmacist-led organization, we recognize Lenalidomide as a breakthrough in hemato-oncology, providing a multifaceted approach to treating plasma cell dyscrasias. Managed through our Mumbai export hub, our formulation is produced in associated oncology-specialized WHO-GMP certified facilities under rigorous containment protocols.
Pharmacological ProfileMechanism of Action (Triple-Action Antineoplastic): Lenalidomide exerts its effects through several distinct pathways:
Direct Cytotoxicity: It binds to Cereblon (CRBN), part of the E3 ubiquitin ligase complex. This triggers the degradation of essential transcription factors (IKZF1 and IKZF3), leading to the apoptosis of malignant cells.
Anti-Angiogenesis: It inhibits the secretion of vascular endothelial growth factor (VEGF), effectively "starving" tumors by preventing the formation of new blood vessels.
Immunomodulation: It stimulates the activation and proliferation of T-cells and Natural Killer (NK) cells, enhancing the body's own immune response against cancerous cells.
Clinical Indications:
Multiple Myeloma (MM): Used in combination with Dexamethasone as a standard of care for both newly diagnosed and relapsed/refractory MM.
Myelodysplastic Syndromes (MDS): Specifically for patients with transfusion-dependent anemia due to low- or intermediate-1-risk MDS associated with a deletion 5q cytogenetic abnormality.
Mantle Cell Lymphoma (MCL): For patients whose disease has relapsed or progressed after two prior therapies.
Pharmacokinetic Profile: Lenalidomide is rapidly absorbed following oral administration with a bioavailability of approximately 67%. It is primarily excreted unchanged by the kidneys, making renal function monitoring a clinical priority for dose adjustment.
| Feature | Specification |
| Active Ingredient | Lenalidomide |
| Available Strengths | 5 mg, 10 mg, 15 mg, 25 mg |
| Therapeutic Class | Immunomodulatory Agent (IMiD) |
| Regulatory Status | WHO-GMP Oncology Certified |
| Primary Packaging | Alu-Alu Blister (Unit Dose) |
| Dosage Form | Hard Gelatin Capsule |
| Storage | Store at 20°C to 25°C; Strictly Protect from Moisture |
As a pharmacist, you understand that Lenalidomide is classified as a highly potent and teratogenic compound. It requires a specialized Risk Evaluation and Mitigation Strategy (REMS) or equivalent pregnancy prevention program in many jurisdictions. We utilize Alu-Alu blister packaging as a mandatory standard for all exports to Africa, LATAM, and SEA. This ensures a 100% moisture barrier and prevents accidental exposure. Our Mumbai logistics team handles these high-value oncology shipments with "Track & Trace" protocols to ensure security and stability in Zone IVb climates.
Product Price :Get Latest Price
Product Details:| Strength | 6 mg/ml |
| Pack Size | 3 ml |
| Brand | Novo Nordisk |
| Composition | Liraglutide |
| Indication | Type 2 Diabetes |
| Form | Pre-filled Pen |
| Storage Temp | 2-8 deg C |
| Shelf Life | 18 months |
| Prescription | Prescription Only |
Healthy Inc offers LIVOHIDE, a high-potency Third-Generation Fluoroquinolone Antibiotic. Containing Levofloxacin, LIVOHIDE provides broad-spectrum bactericidal activity against a wide range of Gram-positive and Gram-negative pathogens. It is a clinical priority for the treatment of Community-Acquired Pneumonia (CAP), Complicated Urinary Tract Infections (cUTI), Acute Pyelonephritis, and Skin and Soft Tissue Infections. As a specialized Indian export partner, we supply this essential anti-infective to respiratory clinics and general hospital networks in global pharmaceutical markets.
Bactericidal Efficiency: Works by inhibiting bacterial DNA gyrase and topoisomerase IV, effectively preventing DNA replication and repair.
Manufacturing: Produced in associated WHO-GMP certified sterile facilities specialized in Large Volume Parenterals (LVP), ensuring 100% sterility, high molecular purity, and precise 5 mg/ml concentration in a 100 ml ready-to-use infusion.
Climate Stability: Validated for Zone IVb (Hot/Humid) conditions, ensuring the chemical integrity and antimicrobial potency of the molecule across Africa, LATAM, and SEA markets.
Regulatory Support: Full technical documentation available, including CTD/eCTD Dossiers, to streamline the registration of essential hospital-grade antibiotics.
Accepting B2B inquiries for contract manufacturing, bulk supply, and global distribution partnerships from our Mumbai export hub.
Available strengths and packaging? We supply LIVOHIDE in 100 ml presentations containing 500 mg of Levofloxacin. It is available in high-quality Non-PVC / Self-Collapsible Bags or USP Type I glass bottles. Every batch undergoes rigorous HPLC-based assay testing and sterility validation.
Support for tropical export? Yes. LIVOHIDE is Zone IVb stability-tested. We utilize light-protected secondary packaging and specialized export-grade outer cartons to ensure product integrity during international transit to high-temperature regions.
Registration assistance provided? We provide complete Regulatory Technical Files (CTD) and Certificates of Analysis (COA) to facilitate local health authority approvals and government hospital tender participations in your specific territory.
Small-volume or mixed orders? We specialize in mixed-container consolidation, allowing you to combine LIVOHIDE with other critical care infusions (such as Linezolid, Metronidazole, or Ciprofloxacin) in a single, cost-effective shipment.
Direct sourcing? Products are sourced through Healthy Life Group’s associated WHO-GMP manufacturing units, ensuring competitive direct-from-factory pricing and strict quality control oversight for essential anti-infective therapies.
Approx. Rs 41.16 / StripGet Latest Price
Product Details:| Strength | 0.5 mg |
| Brand | Dexona |
| Form | Tablet |
| Packaging Size | 10 tablets |
| Usage | Arthritis |
| Packaging Type | Strip |
Healthy Inc offers DEXATORE, a high-potency Glucocorticoid and essential Corticosteroid injectable. Containing Dexamethasone Sodium Phosphate, DEXATORE is a clinical cornerstone for the rapid management of severe inflammatory and allergic conditions. It is a critical-care priority for treating Anaphylaxis, Cerebral Edema, Acute Asthma, and as an adjunctive therapy in Septic Shock. As a specialized Indian export partner, we supply this high-efficacy emergency medicine to hospital networks and trauma centers across global pharmaceutical markets.
Manufacturing: Produced in associated WHO-GMP certified sterile facilities, ensuring 100% sterility, high molecular purity, and precise concentration for IV, IM, or intra-articular administration.
Climate Stability: Validated for Zone IVb (Hot/Humid) conditions, ensuring therapeutic potency and molecular integrity across Africa, LATAM, and SEA markets.
Regulatory Support: Full technical documentation available, including CTD/eCTD Dossiers to streamline the registration process for essential corticosteroid injectables.
Accepting B2B inquiries for contract manufacturing, bulk supply, and global distribution partnerships from our Mumbai export hub.
Available strengths and quality? We supply DEXATORE in 2ml ampoules (4mg/ml, providing 8mg total dose). Every batch undergoes rigorous HPLC-based assay testing, sterility validation, and bacterial endotoxin testing (BET) to meet international pharmacopoeia standards.
Support for tropical export? Yes. DEXATORE is Zone IVb stability-tested. We utilize neutral USP Type I glass ampoules and specialized export-grade secondary packaging to prevent chemical degradation during international transit to high-temperature regions.
Registration assistance provided? We provide complete Regulatory Technical Files (CTD) and Certificates of Analysis (COA) to facilitate local health authority approvals and hospital tender participations in your specific region.
Small-volume or mixed orders? We specialize in mixed-container consolidation, allowing you to combine DEXATORE with other therapeutic categories (such as antibiotics, PPI injectables, or emergency critical care medicines) in a single, cost-effective shipment.
Direct manufacturing? Products are sourced through Healthy Life Group’s associated WHO-GMP manufacturing units, ensuring competitive direct-from-factory pricing and strict quality control oversight.
Approx. Rs 167.21 / PieceGet Latest Price
Product Details:| Strength | 1g/5ml |
| Brand | Carnishor |
| Packaging Size | 5 Ampoules |
| Dosage Form | Ampoule |
| Route of Administration | IV Use Only |
| Usage/Application | Dialysis |
| Manufacturer | Torrent |
Healthy Inc offers POCOLEV, a high-potency Fluoroquinolone Antibacterial presented as a ready-to-use Intravenous (IV) infusion. Containing Levofloxacin 500 mg in a 100 mL isotonic solution, POCOLEV is a clinical priority for treating severe bacterial infections, including Community-Acquired Pneumonia (CAP), Nosocomial Pneumonia, Complicated Urinary Tract Infections (cUTI), and Acute Pyelonephritis. As a specialized Indian export partner, we supply this essential broad-spectrum antibiotic to intensive care units and multi-specialty hospitals in global pharmaceutical markets.
Broad-Spectrum Efficacy: Acts by inhibiting bacterial DNA gyrase and topoisomerase IV, essential for DNA replication, transcription, and repair. It provides excellent coverage against both Gram-positive and Gram-negative pathogens, including Streptococcus pneumoniae and Pseudomonas aeruginosa.
Ready-to-Use (RTU) Presentation: The 100 mL infusion format eliminates the need for manual reconstitution and dilution, reducing the risk of medication errors and microbial contamination in high-pressure clinical settings.
Manufacturing Excellence: Produced in associated WHO-GMP certified sterile facilities. The solution is formulated under strict aseptic conditions to ensure 100% sterility, high molecular purity, and precise pH balance for safe IV administration.
Climate Stability: Validated for Zone IVb (Hot/Humid) conditions; the formulation is stabilized to prevent degradation and ensure chemical integrity across Africa, LATAM, and SEA markets.
Accepting B2B inquiries for contract manufacturing, bulk supply, and hospital distribution partnerships from our Mumbai export hub.
Available strengths and packaging? We supply POCOLEV in the standard 500 mg / 100 mL and 750 mg / 150 mL strengths. It is available in high-quality USP Type I glass bottles or specialized Non-PVC (BFS) IV bags. Every batch undergoes rigorous HPLC-based assay testing and sterility validation.
Support for tropical export? Yes. POCOLEV is Zone IVb stability-tested. We utilize specialized secondary packaging and light-shielding materials to protect the Levofloxacin molecule from photodegradation during international transit to high-temperature regions.
Registration assistance provided? We provide complete Regulatory Technical Files (CTD) and Certificates of Analysis (COA) to facilitate local health authority approvals and government healthcare or institutional tender participations in your specific territory.
Small-volume or mixed orders? We specialize in mixed-container consolidation, allowing you to combine POCOLEV with other critical care antibiotics (such as Meropenem, Ceftriaxone, or Metronidazole) in a single, cost-effective shipment.
Direct sourcing? Products are sourced through Healthy Life Group’s associated WHO-GMP specialized manufacturing units, ensuring competitive direct-from-factory pricing and strict quality control oversight for essential anti-infective care.
Explore More Products
© Healthy Inc. All Rights Reserved (Terms of Use)
Developed and Managed by IndiaMART InterMESH Limited