Mumbai, Maharashtra
GST No. 27AAFFH3493R3ZK
Product Price :Get Latest Price
Product Details:| Treatment Type | Breast Cancer |
| Dosage Form | Injection |
| Brand | Emcure |
| Composition | Bleomycin |
| Manufacturer | Celon Laboratories |
| Strength | 10 mg |
| Packaging Size | 15 unit |
| Storage | 2-8 degree c |
| Packing Type | Vial |
| Shelf Life | 24 months |
Healthy Inc offers NUAVOMIN, a high-efficiency 5-HT₃ Receptor Antagonist designed for the rapid prevention and management of emesis. Containing Ondansetron, NUAVOMIN is a clinical priority for the prevention of Nausea and Vomiting associated with highly emetogenic cancer chemotherapy, radiotherapy, and post-operative recovery. As a specialized Indian export partner, we supply this essential antiemetic to oncology centers, surgical units, and general hospital networks in global pharmaceutical markets.
Clinical Precision: Acts by selectively blocking serotonin receptors in both the peripheral vagus nerve terminals and the central chemoreceptor trigger zone (CTZ), providing potent control over the vomiting reflex without the extrapyramidal side effects of traditional antiemetics.
Manufacturing: Produced in associated WHO-GMP certified sterile facilities. The formulation ensures 100% sterility, high molecular purity, and a standard 2 mg/mL concentration for Intravenous (IV) or Intramuscular (IM) administration.
Climate Stability: Validated for Zone IVb (Hot/Humid) conditions; the formulation is stabilized to ensure chemical integrity and potency across the tropical climates of Africa, LATAM, and SEA markets.
Regulatory Support: Full technical documentation available, including CTD/eCTD Dossiers, to streamline the registration of essential supportive 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 NUAVOMIN in 2 mL ampoules (containing 4 mg) and 4 mL ampoules (containing 8 mg). Every batch undergoes rigorous HPLC-based assay testing, sterility validation, and pH stability checks to meet international pharmacopoeia standards.
Support for tropical export? Yes. NUAVOMIN is Zone IVb stability-tested. We utilize neutral USP Type I glass ampoules and specialized 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 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 NUAVOMIN with other gastrointestinal or critical care injectables (such as Pantoprazole, Dexamethasone, or various chemotherapy agents) 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.
Product Price :Get Latest Price
Product Details:| Dosage Form | Tablet |
| Strength | 5 mg/ml |
| Certification | WHO GMP |
| Pack size | 1 ml |
| Minimum Batch Size | 5000 units |
| Brand | Cipla |
| Composition | Metoclopramide 5 mg/ml |
| Route | IV |
| Plant Type | Beta Lactam |
| Usage | Hospital |
| Form | Injection |
| Business Model | Third Party |
| Packaging type | Ampoule |
| Plant Location | Baddi |
| Shelf life | 24 months |
| Regulatory Support | Product Dossier |
| Storage | Below 25°C |
| Target Market | Domestic |
Healthy Inc offers Metoclopramide Hydrochloride Drops, a potent Prokinetic and Antiemetic agent. As a pharmacist, you recognize Metoclopramide for its unique dual mechanism of action that coordinates upper gastrointestinal motility while simultaneously suppressing the vomiting center in the brain. Managed through our Mumbai export hub, these concentrated drops are manufactured in WHO-GMP certified facilities, providing a precise dosing solution for pediatric and geriatric patients where swallowing tablets is difficult.
We are offering ready stock of below top 30 Indian brands & Generic Brands.
Perinorm Drops, Metoz (Variant), Reglan (Generic), Vominorm, Promet, Emidoxin, Meclop, Mecloz, Metonorm, Periset, Metpure-D, Metstart-D, Metsift-D, Metford-D, Metnova-D, Metgard-D, Metzest-D, Metlap-D, Metspan-D, Metshine-D, Metbrite-D, Metmed-D, Metsafe-D, Metplus-D, Methealth-D, Metoclopramide Healthy, Metoclopramide Ajanta, Metoclopramide Alkem, Metoclopramide Sun, Metoclopramide PMBJP.
Product Usage & AdministrationTherapeutic Goal: To stimulate upper GI motility and prevent nausea and vomiting by increasing the resting tone of the lower esophageal sphincter.
Common Applications:
Diabetic Gastroparesis: Relieving symptoms of delayed gastric emptying (nausea, vomiting, and bloating).
GERD (Gastroesophageal Reflux Disease): Facilitating gastric emptying to prevent acid reflux.
Nausea & Vomiting: Effective for chemotherapy-induced or post-operative emesis.
Diagnostic Aid: Used to facilitate small bowel intubation or radiologic examinations.
Administration: Oral. Ideally administered 30 minutes before meals and at bedtime.
Therapeutic Category
Primary Classification: Prokinetic Agent / Antiemetic.
Pharmacological Class: Dopamine ($D_2$) Receptor Antagonist.
ATC Code: A03FA01.
Metoclopramide exerts its effects through a complex interaction with dopaminergic and serotonergic receptors:
Central Antiemetic Effect: It blocks Dopamine ($D_2$) receptors in the Chemoreceptor Trigger Zone (CTZ) of the area postrema, effectively raising the threshold for vomiting.
Peripheral Prokinetic Effect: It antagonizes peripheral $D_2$ receptors and enhances the response to Acetylcholine in the upper GI tract. This leads to:
Increased lower esophageal sphincter (LES) tone.
Increased gastric contractions (antral) and peristalsis.
Relaxation of the pyloric sphincter and duodenal bulb for faster emptying.
Serotonergic Modulation: At higher doses, it also acts as a $5\text{-}HT_3$ antagonist and $5\text{-}HT_4$ agonist, further supporting its anti-nausea profile.
| Feature | Specification |
| Active Ingredient | Metoclopramide Hydrochloride |
| Concentration | 5 mg per 1 ml (Concentrated Drops) |
| Regulatory Status | WHO-GMP Certified Production |
| Primary Packaging | 10 ml / 15 ml / 30 ml Amber Glass Bottles with Calibrated Dropper |
| Flavor Profile | Sweetened Mint / Fruit (Masks the bitter hydrochloride salt) |
| Storage | Store below 30°C; Protect from light |
Approx. Rs 12.73 / BoxGet Latest Price
Product Details:| Dosage form | Tablet |
| Strength | 4 mg |
| Brand | Cipla |
| Pack size | 10 tablets |
| Packaging type | Blister |
| Prescription | Rx only |
| Shelf life | 24 months |
| Usage | Nausea |
| Composition | Ondansetron |
Healthy Inc offers ONDANAUS, a high-efficiency 5-HT₃ Receptor Antagonist designed for the rapid prevention and management of emesis. Containing Ondansetron, ONDANAUS is a clinical priority for the prevention of Nausea and Vomiting associated with highly emetogenic cancer chemotherapy, radiotherapy, and post-operative recovery. As a specialized Indian export partner, we supply this essential antiemetic to oncology centers, surgical units, and general hospital networks in global pharmaceutical markets.
Clinical Precision: Acts by selectively blocking serotonin receptors in both the peripheral vagus nerve terminals and the central chemoreceptor trigger zone (CTZ), providing potent control over the vomiting reflex without the extrapyramidal side effects of traditional antiemetics.
Manufacturing: Produced in associated WHO-GMP certified sterile facilities. The formulation ensures 100% sterility, high molecular purity, and a standard 2 mg/mL concentration for Intravenous (IV) or Intramuscular (IM) administration.
Climate Stability: Validated for Zone IVb (Hot/Humid) conditions; the formulation is stabilized to ensure chemical integrity and potency across the tropical climates of Africa, LATAM, and SEA markets.
Regulatory Support: Full technical documentation available, including CTD/eCTD Dossiers, to streamline the registration of essential supportive 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 ONDANAUS in 2 mL ampoules (containing 4 mg) and 4 mL ampoules (containing 8 mg). Every batch undergoes rigorous HPLC-based assay testing, sterility validation, and pH stability checks to meet international pharmacopoeia standards.
Support for tropical export? Yes. ONDANAUS is Zone IVb stability-tested. We utilize neutral USP Type I glass ampoules and specialized 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 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 ONDANAUS with other gastrointestinal or critical care injectables (such as Pantoprazole, Dexamethasone, or various chemotherapy agents) 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 759.38 / VialGet Latest Price
Product Details:| Dosage Form | Injection |
| 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 |
| Strength | 500 mg |
Healthy Inc offers Pemetrexed Injection IP, a potent Antifolate Antineoplastic agent essential for advanced oncological care. Containing Pemetrexed Disodium 100 mg, this formulation is a clinical priority for the treatment of Malignant Pleural Mesothelioma (in combination with Cisplatin) and as a 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 centers and specialized infusion clinics in global pharmaceutical markets.
Multitargeted Enzyme Inhibition: Functions by disrupting folate-dependent metabolic processes essential for cell replication. It inhibits three key enzymes: thymidylate synthase (TS), dihydrofolate reductase (DHFR), and glycinamide ribonucleotide formyltransferase (GARFT), effectively arresting the purine and pyrimidine synthesis required for DNA/RNA formation.
Manufacturing Excellence: Produced in associated WHO-GMP certified specialized oncology facilities. The Lyophilized Powder for injection ensures 100% sterility, high molecular purity, and rapid reconstitution for Intravenous (IV) infusion.
Clinical Protocol Support: Pemetrexed requires specific premedication (Folic Acid, Vitamin B12, and Corticosteroids) to reduce toxicity; our technical documentation provides clear guidance for clinical teams to ensure patient safety.
Climate Stability: Validated for Zone IVb (Hot/Humid) conditions. The lyophilized form is highly stable and engineered to maintain chemical integrity across the demanding 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 100 mg vial and the 500 mg vial. 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. Pemetrexed is Zone IVb stability-tested. We utilize neutral USP Type I glass vials and specialized moisture-resistant secondary packaging to ensure the stability of the cytotoxic molecule 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 oncology tender participations in your specific territory.
Small-volume or mixed orders? We specialize in mixed-container consolidation, allowing you to combine Pemetrexed 100 mg with other oncology essentials (such as Cisplatin, Carboplatin, or supportive care medications like Dexamethasone and Ondansetron) 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 50 / PieceGet Latest Price
Product Details:| Strength | 40 mg/ml |
| Pack Size | 1 ml |
| Pack Type | Ampoule |
| Composition | Artemether |
| Injection Route | IM |
| Application | Severe Malaria |
| Brand | Larinate |
| Shelf Life | 18 Months |
Healthy Inc offers Artemether Injection, a high-potency lipid-soluble artemisinin derivative and a powerful blood schizonticide. Available in both 40 mg (pediatric/moderate) and 80 mg (adult/severe) strengths, this injectable is a clinical priority for the treatment of severe malaria, including multi-drug resistant Plasmodium falciparum and cerebral malaria. As a specialized Indian export partner, we supply this fast-acting antimalarial to tropical medicine centers and public health departments globally.
Rapid Parasite Clearance: Artemether acts by generating reactive free radicals within the parasite's food vacuole, leading to the rapid destruction of the malaria parasite's membranes. It ensures a swift reduction in parasitemia, which is critical in preventing the progression of severe malaria and reducing mortality rates.
Targeted for Severe & Resistant Cases: Specifically indicated for cases where oral medication is not feasible and for strains that have developed resistance to traditional treatments like chloroquine or quinine.
Manufacturing Excellence: Produced in associated WHO-GMP certified sterile facilities. The solution is formulated in a refined oil base to ensure a sustained therapeutic effect following Deep Intramuscular (IM) administration.
Climate-Adaptive Stability: Artemether is inherently more stable than water-soluble derivatives in high-temperature environments. Validated for Zone IVb (Hot/Humid) conditions, it is vacuum-sealed in amber USP Type I glass ampoules to prevent photo-degradation during transit to Africa, LATAM, and SEA markets.
Accepting B2B inquiries for high-volume contract manufacturing, bulk supply, and government hospital tender participation from our Mumbai export hub.
B2B Trade Specifications| Feature | Specification |
|---|---|
| Active Ingredient | Artemether |
| Available Strengths | 40 mg / 1 mL; 80 mg / 1 mL |
| Therapeutic Class | Antimalarial (Artemisinin Derivative) |
| Regulatory Status | WHO-GMP Certified Production |
| Primary Packaging | Amber USP Type I Glass Ampoule |
| Route of Admin. | Deep Intramuscular (IM) Only |
| Storage | Store below 30°C; Protect from light |
Logistics & Export Optimization As a pharmacist-led firm, we understand that antimalarials are time-sensitive medical essentials. We ensure that our export shipments utilize light-protected, impact-resistant secondary packaging to maintain the molecular integrity of the oily solution during the rigors of international transit.
Registration & Compliance Support We provide complete Regulatory Technical Files (CTD) and batch-specific Certificates of Analysis (COA). Our documentation is specifically designed to facilitate rapid health authority approvals and meet the strict requirements of international NGO and government procurement cycles.
Approx. Rs 8,130.00 / VialGet Latest Price
Product Details:| Brand | Cadila Pharmaceuticals |
| Strength | 0.3 mL |
| Packaging Size | 10 ampoules |
| Composition | Heat killed Mycobacterium w |
| Packaging Type | Vial |
| Usage/Application | Hospital |
| Prescription | Prescription |
| Shelf Life | 18 months |
| Storage Condition | 2–8°C |
| Country of Origin | India |
Healthy Inc offers SEPSIVAC, a pioneering immunomodulator containing heat-killed Mycobacterium w ($Mw$). This breakthrough therapeutic is a clinical priority for the management of Gram-negative sepsis and associated Systemic Inflammatory Response Syndrome (SIRS). It is specifically designed to restore immune balance in critically ill patients, reducing mortality and the duration of mechanical ventilation in Intensive Care Units (ICUs).
Dual Action Immunomodulation: Unlike standard antibiotics, SEPSIVAC works by modulating the host's immune response. It helps down-regulate the "cytokine storm" (pro-inflammatory phase) while boosting the body’s ability to clear the infection (anti-inflammatory/compensatory phase).
Clinical Efficacy: Extensively used as an adjunct therapy in severe sepsis and septic shock. It has demonstrated significant results in improving organ function and increasing the number of "ventilator-free days" for patients with severe respiratory distress.
Manufacturing Excellence: Produced in state-of-the-art WHO-GMP certified facilities (Cadila Pharmaceuticals). The formulation is processed under stringent aseptic conditions to ensure 100% sterility and consistent antigenic potency.
Global Recognition: Recognized as a "first-in-the-world" drug for sepsis management, SEPSIVAC is a high-demand export for healthcare systems looking to enhance critical care outcomes in Africa, LATAM, and SEA markets.
Accepting B2B inquiries for hospital supply, institutional tender participation, and global distribution from our Mumbai export hub.
Available strengths and packaging?
We supply SEPSIVAC as a sterile suspension in 0.3 mL or 0.5 mL single-dose vials. Every batch undergoes rigorous quality control and immunological validation to ensure the concentration of heat-killed bacilli meets the specified therapeutic standard.
Support for tropical export?
Yes. While SEPSIVAC is typically stored under cold chain (2°C to 8°C), our export logistics team utilizes validated thermal shippers to maintain temperature integrity during international transit, ensuring the product reaches its destination with full potency.
Registration assistance provided?
We provide comprehensive Regulatory Technical Files (CTD) and clinical data summaries to facilitate local health authority approvals and government healthcare or ICU-specialty tender participations.
Mixed-container consolidation?
Through our Mumbai hub, we can consolidate SEPSIVAC with other critical care injectables (such as Meropenem, Vasopressin, or Albumin) to provide a complete, cost-effective solution for specialized ICU departments.
Approx. Rs 77.17 / VialGet Latest Price
Product Details:| Strength | 0.25% |
| Vial Volume | 4 ml |
| With Dextrose | Plain |
| Route | Epidural |
| Pack Type | Ampoule |
| Brand | Sensorcaine |
| Preservative | With Preservative |
| Pack Size | Box of 5 |
| Storage | Store below 25°C |
Healthy Inc offers Bupivacaine Hydrochloride Injection, a high-precision amino-amide local anesthetic. Known for its potent and prolonged duration of action, Bupivacaine is a clinical staple for surgical anesthesia and post-operative pain management. As a specialized Indian export partner, we supply this essential anesthetic in various concentrations and formats, including Plain and Heavy (with Dextrose), to surgical centers and anesthesia departments globally.
Mechanism of Action: Bupivacaine acts by blocking the generation and conduction of nerve impulses. It increases the threshold for electrical excitation in the nerve by slowing the propagation of the nerve impulse and by reducing the rate of rise of the action potential. This results in a reversible loss of sensation and, at higher concentrations, motor blockade.
Extended Duration of Action: One of the most significant advantages of Bupivacaine is its long half-life and duration (typically 3 to 9 hours depending on the site of injection). This makes it the drug of choice for long surgical procedures and continuous pain relief via catheter.
Clinical Versatility: Indicated for Spinal Anesthesia (subarachnoid block), Epidural Anesthesia, peripheral nerve blocks, and local infiltration. The "Heavy" 0.5% formulation (containing Dextrose) is specifically designed to provide predictable hyperbaric spread during spinal procedures.
Manufacturing Excellence: Produced in associated WHO-GMP certified sterile facilities. The solution is formulated with rigorous osmotic and pH controls to ensure patient safety and rapid onset within the localized tissue.
Climate-Adaptive Packaging: Validated for Zone IVb (Hot/Humid) conditions. Encapsulated in USP Type I glass ampoules or vials to ensure 100% sterility and chemical stability during international transit to Africa, LATAM, and SEA markets.
Accepting B2B inquiries for hospital supply, anesthesia-specialty tender participation, and global distribution from our Mumbai export hub.
B2B Technical Specifications| Feature | Specification |
| Active Ingredient | Bupivacaine Hydrochloride |
| Common Concentrations | 0.25% (2.5 mg/mL) / 0.5% (5 mg/mL) |
| Available Formats | Plain / Heavy (with 80 mg Dextrose) |
| Therapeutic Class | Local Anesthetic (Amide-type) |
| Regulatory Status | WHO-GMP Certified Production |
| Primary Packaging | USP Type I Glass Ampoule or Vial |
| Storage | Store below 30°C; Do Not Freeze |
Logistics & Stability Management
As a pharmacist-led firm, we understand that anesthetics require uncompromising purity. We utilize specialized secondary packaging to protect the glass containers from physical shock and temperature fluctuations during multi-modal international transport. We ensure that our Bupivacaine Heavy solutions remain clear and free of precipitation, maintaining the precise density required for successful spinal blocks.
Approx. Rs 72.24 / VialGet Latest Price
Product Details:| Strength | 40 mg/ml |
| Volume | 2 ml |
| Brand | Genticyn |
| Composition | Gentamicin |
| Route of Administration | IM |
| Pack Type | Ampoule |
Healthy Inc offers Gentamicin Sulphate Injection in the specialized 20 mg / 2 mL (10 mg/mL) concentration. This lower-strength formulation is a clinical priority for pediatric and neonatal care, where precise dosing is critical to avoid toxicity while ensuring bactericidal efficacy. As a pharmacist-led export partner, we supply this essential aminoglycoside to pediatric hospitals and maternal care centers globally from our Mumbai export hub.
Bactericidal Precision: Gentamicin acts by irreversibly binding to the 30S ribosomal subunit of the bacteria, inhibiting protein synthesis and causing cell death. It remains highly effective against a broad spectrum of aerobic Gram-negative pathogens, including Pseudomonas aeruginosa, Klebsiella, and Proteus spp.
Clinical Criticality in Neonatology: The 20 mg/2 mL strength is specifically utilized for treating severe neonatal infections, including Neonatal Sepsis, meningitis, and complicated urinary tract infections. It is often used in combination with a $\beta$-lactam antibiotic for synergistic effect.
Narrow Therapeutic Index Management: Because aminoglycosides carry risks of ototoxicity and nephrotoxicity, this 10 mg/mL concentration allows healthcare providers to draw up exact pediatric doses more accurately than higher-strength adult formulations.
Manufacturing Excellence: Produced in associated WHO-GMP certified sterile facilities. The solution is formulated with precise pH buffering and antioxidants (such as Sodium Metabisulfite) to ensure long-term stability and 100% molecular bioavailability.
Accepting B2B inquiries for high-volume hospital supply, pediatric-specialty tenders, and international distribution.
B2B Technical Specifications| Feature | Specification |
| Active Ingredient | Gentamicin Sulphate |
| Strength | 20 mg / 2 mL (10 mg/mL) |
| Therapeutic Class | Aminoglycoside Antibiotic |
| Regulatory Status | WHO-GMP Certified Production |
| Primary Packaging | USP Type I Clear Glass Ampoule (2 mL) |
| Route of Admin. | Intramuscular (IM) or Intravenous (IV) |
| Storage | Store below 30°C; Do Not Freeze |
As a pharmacist-led firm, we understand that pediatric antibiotics are high-demand essential medicines. We utilize reinforced secondary packaging to protect the 2 mL glass ampoules from physical shock during multi-modal international transit. Our logistics team ensures that shipments to Africa, LATAM, and SEA are handled with climate-controlled protocols to maintain chemical stability in Zone IVb environments.
Registration & Compliance SupportWe provide complete Regulatory Technical Files (CTD) and batch-specific Certificates of Analysis (COA). Our documentation is designed to meet the rigorous safety standards of international pediatric boards and national health authorities, facilitating smooth entry into government healthcare systems.
Pediatric Portfolio ConsolidationThrough our Mumbai hub, we can consolidate Gentamicin 20 mg with other pediatric essentials—such as Amikacin (Pediatric), Ceftriaxone 250 mg, and Sterile Water for Injection (2 mL PolyPacks)—providing a comprehensive clinical portfolio in a single, cost-effective shipment.
Approx. Rs 278.00 / BoxGet Latest Price
Product Details:| Strength | 5 g/10 ml |
| Pack Size | 10 ml Vial |
| Dosage Form | Injection |
| Route | IV |
| Storage | Below 25°C |
| Usage | Hospital |
| Brand | Hepamerz |
| Shelf Life | 18 months |
Healthy Inc offers L-Ornithine L-Aspartate (LOLA), a high-precision hepato-protective agent. Formulated as a concentrated sterile solution, LOLA is a clinical priority for the management of severe liver dysfunction and metabolic encephalopathy. As a specialized Indian export partner, we supply this advanced amino acid complex to tertiary care hospitals and hepatology centers globally from our Mumbai export hub.
Dual-Action Ammonia Detoxification: LOLA works by providing two critical substrates for the detoxification of ammonia in the body:
L-Ornithine: Acts as a substrate for the Urea Cycle in periportal hepatocytes, converting toxic ammonia into urea.
L-Aspartate: Stimulates Glutamine synthesis in perivenous hepatocytes and muscles, further neutralizing ammonia into non-toxic glutamine.
Clinical Criticality: Indicated for the treatment of Hepatic Encephalopathy (HE), both in latent and overt stages, and as a supportive therapy in chronic liver diseases such as Liver Cirrhosis, fatty liver, and drug-induced hepatotoxicity. It effectively lowers blood ammonia levels, improving the neurological status of patients.
Metabolic Support: Beyond ammonia clearance, the combination promotes the regeneration of liver cells and improves the energy balance of the diseased liver.
Manufacturing Excellence: Produced in associated WHO-GMP certified sterile facilities. Our formulation is engineered with precise osmotic balancing and pH control to ensure safety during high-dose Intravenous (IV) Infusion.
| Feature | Specification |
|---|---|
| Active Ingredients | L-Ornithine L-Aspartate |
| Strength | 5 gm per 10 mL (0.5 gm/mL) |
| Therapeutic Class | Hepato-protective / Amino Acid Complex |
| Regulatory Status | WHO-GMP Certified Production |
| Primary Packaging | USP Type I Clear Glass Ampoule / Vial |
| Route of Admin. | Intravenous (IV) Infusion Only (Dilute before use) |
| Storage | Store below 30°C; Do not freeze |
As a pharmacist-led organization, we understand that high-concentration amino acid solutions require rigorous clarity testing to ensure the absence of precipitates. We utilize USP Type I glass to prevent any leaching and maintain the purity of the L-isomers. Our logistics team optimizes shipments for Zone IVb climates, ensuring that the product remains stable and effective during international transit to Africa, LATAM, and SEA markets.
Product Price :Get Latest Price
Product Details:| Usage | IV Infusion |
| Brand | Alburel |
| Pack Size | 100 ml Vial |
| Strength | 20 g/100 ml |
| Country of Origin | India |
| Prescription Type | Prescription |
| Storage Temp | 2–25°C |
| Pharmacopoeia | IP |
| Albumin Source | Human Plasma |
Healthy Inc offers Human Albumin Injection, a high-purity sterile solution of albumin derived from pooled human venous plasma. As a specialized Indian export partner, we supply this critical plasma expander and protein replacement therapy to Intensive Care Units (ICUs), burn centers, and surgical departments globally from our Mumbai export hub.
Oncotic Pressure Regulation: Albumin is responsible for 70–80% of the colloid osmotic pressure of human plasma. It functions by drawing extravascular fluid into the intravascular compartment, making it a clinical priority for restoring blood volume without the risk of fluid overload associated with crystalloids.
Molecular Transport & Antioxidant Role: Beyond volume expansion, Albumin acts as a high-capacity carrier for hormones, fatty acids, and drugs. It also serves as a potent circulating antioxidant and a buffer for acid-base balance in critically ill patients.
Clinical Criticality: Indicated for the treatment of Hypovolemic Shock, severe Hypoalbuminemia (resulting from liver failure or nephrotic syndrome), and the management of Acute Respiratory Distress Syndrome (ARDS). It is also a staple in large-volume paracentesis and the treatment of severe burns.
Manufacturing Excellence: Sourced from associated facilities utilizing advanced Cohn Cold Ethanol Fractionation. The product undergoes rigorous viral inactivation (Pasteurization at 60°C for 10 hours) and ultra-filtration to ensure 100% safety, molecular integrity, and compliance with Ph. Eur. or USP standards.
| Feature | Specification |
| Active Ingredient | Human Albumin (Salt-Poor) |
| Available Strengths | 5% (Iso-oncotic) / 20% & 25% (Hyper-oncotic) |
| Therapeutic Class | Plasma Expander / Blood Derivative |
| Regulatory Status | WHO-GMP / Plasma Master File (PMF) Compliance |
| Primary Packaging | USP Type II Glass Bottle (50 mL / 100 mL) |
| Storage | Store below 25°C; Do Not Freeze; Protect from light |
As a pharmacist-led organization, we understand that plasma derivatives are highly sensitive biologicals. While Human Albumin is stable at room temperature (below 25°C), we utilize validated thermal packaging and real-time temperature loggers for all international shipments to Africa, LATAM, and SEA. This ensures that the protein remains un-denatured and effective throughout the long-haul transit from Mumbai.
Approx. Rs 192.79 / VialGet Latest Price
Product Details:| Strength | 1.5 mg/ml |
| Vial Volume | 2 ml |
| Pack Type | Single Vial |
| Route | IV |
| Usage | Als |
| Packaging Type | Vial |
| Storage | Below 25 C |
| Brand Type | Branded |
| Prescription | Prescription |
Healthy Inc offers SYNACORT, a high-velocity corticosteroid presented as a sterile lyophilized powder for injection. Available in strengths of 100 mg, 200 mg, and 400 mg, SYNACORT is a clinical priority for the immediate management of life-threatening emergencies, including Anaphylactic Shock, Status Asthmaticus, and Acute Adrenal Insufficiency. As a specialized Indian export partner, we supply this essential rescue steroid to emergency departments and ICUs in global pharmaceutical markets.
Rapid-Acting Anti-Inflammatory: As a soluble salt of hydrocortisone, it provides near-instantaneous systemic effects when administered via Intravenous (IV) or Intramuscular (IM) routes. It is the gold standard for stabilizing patients during severe allergic reactions and Addisonian crises.
Manufacturing Excellence: Produced in associated WHO-GMP certified sterile facilities. The Lyophilized (freeze-dried) format ensures the long-term stability of the corticosteroid molecule and allows for rapid, residue-free reconstitution—critical for time-sensitive emergency care.
Clinical Utility: Beyond shock management, it is indispensable for treating severe dermatological conditions, collagen disorders, and as a supportive therapy in hematological malignancies.
Climate Stability: Validated for Zone IVb (Hot/Humid) conditions; the vacuum-sealed USP Type I glass vials and the lyophilized state protect the product from degradation during transit to Africa, LATAM, and SEA markets.
Accepting B2B inquiries for contract manufacturing, bulk supply, and emergency-care tender participations from our Mumbai export hub.
Available strengths and packaging? We supply SYNACORT in 100 mg, 200 mg, and 400 mg vials, typically accompanied by an ampoule of sterile Water for Injection. Every batch undergoes rigorous HPLC-based assay testing and Bacterial Endotoxin Testing (BET) to meet international standards.
Support for tropical export? Yes. SYNACORT is Zone IVb stability-tested. The lyophilized powder form is specifically chosen for export as it is more resilient to temperature fluctuations than liquid steroid formulations, ensuring efficacy upon arrival 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 healthcare or emergency-specialty tender participations.
Small-volume or mixed orders? We specialize in mixed-container consolidation, allowing you to combine SYNACORT with other emergency injectables (such as Adrenaline, Atropine, or Dexamethasone) 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 critical care medications.
Approx. Rs 478.54 / PieceGet Latest Price
Product Details:| Strength | 20 mg/0.2 ml |
| Brand | Clexane |
| Form | Injection |
| Volume | 0.2 ml |
| Salt Type | Enoxaparin sodium |
| Pack Size | 1 syringe |
| Usage | DVT prophylaxis |
| Packaging Type | Pre filled syringe |
| Route of Administration | SC |
| Storage Temperature | Below 25°C |
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Healthy Inc offers XOMPARIN 40, a high-precision Low Molecular Weight Heparin (LMWH). Containing 40 mg of Enoxaparin Sodium in a 0.4 mL pre-filled syringe (PFS), this formulation is a clinical priority for the prevention and treatment of Deep Vein Thrombosis (DVT) and Pulmonary Embolism. As a specialized Indian export partner, we supply this essential anticoagulant to orthopedic, cardiovascular, and surgical departments globally.
Antithrombotic Precision: XOMPARIN 40 acts by accelerating the activity of antithrombin III, selectively inhibiting clotting factors Xa and IIa. It offers a more predictable pharmacological response and a lower risk of heparin-induced thrombocytopenia (HIT) compared to unfractionated heparin.
Manufacturing Excellence: Produced in associated WHO-GMP certified biopharmaceutical facilities. The formulation is processed under strict aseptic conditions to ensure molecular consistency, high anti-Xa activity, and 100% sterility.
User-Centric Design (PFS): Supplied in a Pre-Filled Syringe (PFS) with an ultra-fine needle for Subcutaneous administration. This ensures accurate dosing, reduces the risk of contamination, and facilitates ease of use for both clinical staff and home-care patients.
Climate-Adaptive Logistics: Validated for Zone IVb (Hot/Humid) conditions. While stable at controlled room temperature, our export protocols ensure the product is shielded from extreme thermal spikes during transit to Africa, LATAM, and SEA markets.
Accepting B2B inquiries for contract manufacturing, bulk supply, and government healthcare tender participation from our Mumbai export hub.
B2B Technical Specifications| Feature | Specification |
| Active Ingredient | Enoxaparin Sodium (LMWH) |
| Strength | 40 mg / 0.4 mL |
| Therapeutic Class | Anticoagulant / Antithrombotic |
| Regulatory Status | WHO-GMP Certified Production |
| Primary Packaging | Sterile Pre-Filled Syringe (PFS) |
| Storage | Store below 25°C; Do not freeze |
Logistics & Export Optimization
As a pharmacist-led firm, we understand that biologicals like XOMPARIN 40 require delicate handling. We utilize impact-resistant secondary packaging and temperature-monitored shipping routes to ensure the molecular integrity of the Enoxaparin is maintained from our warehouse in Mumbai to your final destination.
Registration & Documentation Support
We provide complete Regulatory Technical Files (CTD) and batch-specific Certificates of Analysis (COA). Our documentation is specifically designed to facilitate rapid health authority approvals and meet the strict transparency requirements of international procurement agencies.
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