Critical Care

Approx. Rs 65.63 / PieceGet Latest Price

Product Details:

Levocarnitine Injections 1gm
LEVOCARNITINE Injection USP (1 g / 5 ml)

Healthy Inc offers Levocarnitine 1 g, a high-precision Metabolic Modifier and amino acid derivative. Levocarnitine is a clinical priority for the treatment of Primary and Secondary Carnitine Deficiency, particularly in patients with End-Stage Renal Disease (ESRD) undergoing chronic hemodialysis. By facilitating the transport of long-chain fatty acids into mitochondria for energy production, it manages symptoms of carnitine depletion such as muscle weakness, cardiomyopathy, and anemia. As a specialized Indian export partner, we supply this essential metabolic therapy to dialysis centers and nephrology units in global pharmaceutical markets.

• Metabolic Support: Enhances cellular energy metabolism and is frequently utilized in the management of metabolic disorders and acute carnitine depletion caused by valproate toxicity.

• Manufacturing: Produced in associated WHO-GMP certified sterile facilities, ensuring 100% sterility, high molecular purity, and precise 200 mg/ml concentration for Intravenous (IV) or slow bolus administration.

• Climate Stability: Validated for Zone IVb (Hot/Humid) conditions, ensuring the chemical integrity and metabolic potency of the molecule 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 parenteral nutrients and metabolic modifiers.

Accepting B2B inquiries for contract manufacturing, bulk supply, and global distribution partnerships from our Mumbai export hub.

Available strengths and packaging? We supply Levocarnitine in 5 ml ampoules/vials containing 1000 mg (1 g). Every batch undergoes rigorous HPLC-based assay testing and sterility validation to meet USP and international standards.

Support for tropical export? Yes. Our formulation is Zone IVb stability-tested. We utilize neutral USP Type I glass and specialized export-grade secondary packaging to prevent molecular 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 nephrology tender participations in your specific territory.

Small-volume or mixed orders? We specialize in mixed-container consolidation, allowing you to combine Levocarnitine with other nephrology injectables (such as Iron Sucrose, Erythropoietin, or Vitamin D3) 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 critical care therapies.

Approx. Rs 629.65 / VialGet Latest Price

Product Details:

meropenem 500 mg + sodium carbonate 45.1 mg
MEROVOLVE 0.5G Injection (Meropenem for Injection USP 500 mg)

Healthy Inc offers MEROVOLVE 0.5G, a high-precision, ultra-broad-spectrum Carbapenem Antibiotic. Containing Meropenem 500 mg, MEROVOLVE is a clinical priority for the treatment of severe, complicated infections caused by multi-drug resistant (MDR) Gram-positive and Gram-negative bacteria. It is a frontline therapeutic for Nosocomial Pneumonia, Complicated Urinary Tract Infections (cUTI), Intra-abdominal Infections, and Septicemia. As a specialized Indian export partner, we supply this critical-care antibiotic to Intensive Care Units (ICUs) and tertiary care hospital networks in global pharmaceutical markets.

• Clinical Efficacy: Highly resistant to most bacterial beta-lactamases, including extended-spectrum beta-lactamases (ESBLs), making it an essential choice for empirical therapy in critically ill 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) bolus or infusion.

• Climate Stability: Validated for Zone IVb (Hot/Humid) conditions; the lyophilized powder form provides superior resilience to thermal degradation, ensuring potency across Africa, LATAM, and SEA markets.

• Regulatory Support: Full technical documentation available, including CTD/eCTD Dossiers, to streamline the registration of high-end hospital-grade 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 MEROVOLVE in the 500 mg (0.5G) strength, as well as 1000 mg (1G) and 250 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. MEROVOLVE 0.5G 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 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 critical-care tender participations in your specific territory.

Small-volume or mixed orders? We specialize in mixed-container consolidation, allowing you to combine MEROVOLVE 0.5G with other critical care injectables (such as Piperacillin-Tazobactam, Linezolid, or Vancomycin) 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 life-saving anti-infectives.

Approx. Rs 12,999.00 / VialGet Latest Price

Product Details:

micafungin 100 mg + sodium chloride 0.9% w/v
MICASHIELD 100 mg Injection (Micafungin for Injection BP/USP)

Healthy Inc offers MICASHIELD 100 mg, a high-potency Echinocandin Antifungal agent. Containing Micafungin Sodium, MICASHIELD is a clinical priority for the treatment of severe, systemic fungal infections, including Invasive Candidiasis, Candidemia, and Esophageal Candidiasis. It is also an essential prophylactic therapy for patients undergoing Hematopoietic Stem Cell Transplantation (HSCT) who are at high risk of fungal overgrowth. As a specialized Indian export partner, we supply this critical-care antifungal to oncology centers, transplant units, and ICUs in global pharmaceutical markets.

• Mechanism of Action: Selectively inhibits the synthesis of 1,3-beta-D-glucan, an essential component of the fungal cell wall, resulting in osmotic instability and cell death (fungicidal against Candida species).

• Manufacturing: Produced in associated WHO-GMP certified sterile facilities specialized in Lyophilization, ensuring 100% sterility, high molecular purity, and rapid reconstitution for Intravenous (IV) infusion.

• Climate Stability: Validated for Zone IVb (Hot/Humid) conditions; the lyophilized powder form is highly stable, ensuring the integrity of the echinocandin molecule across Africa, LATAM, and SEA markets.

• Regulatory Support: Full technical documentation available, including CTD/eCTD Dossiers, to streamline the registration of specialized hospital-grade antifungals.

Accepting B2B inquiries for contract manufacturing, bulk supply, and global distribution partnerships from our Mumbai export hub.

Available strengths and quality? We supply MICASHIELD in the 100 mg strength, as well as 50 mg vials. Every batch undergoes rigorous HPLC-based assay testing, sterility validation, and Bacterial Endotoxin Testing (BET) to meet BP/USP and international pharmacopoeia standards.

Support for tropical export? Yes. MICASHIELD 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 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 specialized hospital tender participations in your specific territory.

Small-volume or mixed orders? We specialize in mixed-container consolidation, allowing you to combine MICASHIELD 100 mg with other critical care injectables (such as Caspofungin, Voriconazole, or various 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 essential life-saving antifungal therapies.

Approx. Rs 8,999.00 / VialGet Latest Price

Product Details:

micafungin 50 mg + sodium chloride 0.9% w/v
MICASHIELD 50 mg Injection (Micafungin for Injection BP/USP)

Healthy Inc offers MICASHIELD 50 mg, a high-precision Echinocandin Antifungal agent. Containing Micafungin Sodium, MICASHIELD is a clinical priority for the treatment of systemic fungal infections, specifically Invasive Candidiasis, Candidemia, and Esophageal Candidiasis. It is also a critical therapeutic for the prophylaxis of Candida infections in patients undergoing hematopoietic stem cell transplantation (HSCT) or those with prolonged neutropenia. As a specialized Indian export partner, we supply this advanced antifungal to oncology centers, transplant units, and intensive care networks in global pharmaceutical markets.

• Targeted Antifungal Action: Selectively inhibits the synthesis of 1,3-beta-D-glucan in the fungal cell wall, providing fungicidal activity against most Candida species, including those resistant to azoles.

• Manufacturing: Produced in associated WHO-GMP certified sterile facilities specialized in Lyophilization, ensuring 100% sterility, high molecular purity, and rapid reconstitution for Intravenous (IV) infusion.

• Climate Stability: Validated for Zone IVb (Hot/Humid) conditions; the lyophilized powder form ensures the stability of the echinocandin 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 hospital-grade 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 MICASHIELD in 50 mg and 100 mg vials. Every batch undergoes rigorous HPLC-based assay testing, sterility validation, and Bacterial Endotoxin Testing (BET) to meet BP/USP and international pharmacopoeia standards.

Support for tropical export? Yes. MICASHIELD 50 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 oncology or transplant hospital tender participations.

Small-volume or mixed orders? We specialize in mixed-container consolidation, allowing you to combine MICASHIELD 50 mg with other antifungal or critical care injectables (such as Caspofungin, Voriconazole, or Meropenem) 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 antifungal therapies.

Approx. Rs 10.32 / PieceGet Latest Price

Product Details:

Phytomenadione Injection (Vitamin K1) IP 1mg Per 0.5ml
Phytomenadione Injection IP (Vitamin K1) 1 mg / 0.5 mL

Healthy Inc offers Phytomenadione Injection IP, an essential procoagulant vitamin and a life-saving therapeutic in neonatal and emergency care. Containing 1 mg of Vitamin K1 per 0.5 mL, this formulation is the clinical gold standard for the prevention and treatment of Vitamin K Deficiency Bleeding (VKDB) in newborns. It is also a critical intervention for treating hemorrhage or threatened hemorrhage associated with prothrombin deficiency induced by coumarin or indandione anticoagulants. As a specialized Indian export partner, we supply this essential nutrient-therapeutic to maternity hospitals, pediatric units, and emergency departments in global pharmaceutical markets.

• Clinical Precision: Functions as an essential cofactor for the hepatic synthesis of coagulation factors II (prothrombin), VII, IX, and X. Its rapid action when administered via Intramuscular (IM) or Subcutaneous routes makes it an indispensable component of neonatal care protocols.

• Manufacturing Excellence: Produced in associated WHO-GMP certified sterile facilities. The solution is formulated as a sterile aqueous colloidal solution or emulsion, ensuring 100% sterility and high molecular stability for safe administration.

• Light Protection: Since Vitamin K1 is highly photosensitive, our formulation is processed under specialized light-controlled conditions and filled into high-quality amber glass to prevent photodegradation and ensure full potency.

• Climate Stability: Validated for Zone IVb (Hot/Humid) conditions; the formulation is stabilized to maintain its chemical integrity and procoagulant activity across Africa, LATAM, and SEA markets.

Accepting B2B inquiries for contract manufacturing, bulk supply, and pediatric distribution partnerships from our Mumbai export hub.

Available strengths and packaging? We supply Phytomenadione in the 1 mg / 0.5 mL neonatal strength and the 10 mg / 1 mL adult strength. 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 amber glass ampoules and light-shielding secondary packaging to protect the Vitamin K1 molecule from UV 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 government healthcare or pediatric tender participations in your specific territory.

Small-volume or mixed orders? We specialize in mixed-container consolidation, allowing you to combine Phytomenadione with other maternal and child health essentials (such as Oxytocin, Gentamicin, or Vitamin D3) 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 neonatal care.

Approx. Rs 210.94 / PieceGet Latest Price

Product Details:

Terlipressin Injection 1000 Mcg (1 Mg/10ml)
TERLIPRESSIN Injection (1 mg / 10 mL)

Healthy Inc offers Terlipressin Injection, a potent synthetic analogue of vasopressin. Containing 1000 mcg (1 mg) of Terlipressin acetate in a 10 mL vial, this formulation is a clinical priority for the emergency management of Acute Variceal Bleeding and Hepatorenal Syndrome (Type 1). As a specialized Indian export partner, we supply this critical-care therapeutic to gastroenterology departments and Intensive Care Units (ICUs) in global pharmaceutical markets.

• Clinical Precision: Acts as a systemic vasoconstrictor with high selectivity for the splanchnic circulation. By reducing portal venous pressure, it effectively controls bleeding from esophageal varices, providing a vital bridge to endoscopic therapy or surgery.

• Renal Support: In Hepatorenal Syndrome, Terlipressin improves renal blood flow and glomerular filtration rate by reversing systemic vasodilation, making it a cornerstone therapy in liver-related emergencies.

• 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 a precise pH balance for safe Intravenous (IV) bolus or infusion.

• Climate Stability: Validated for Zone IVb (Hot/Humid) conditions. While Terlipressin often requires refrigerated storage (2°C to 8°C), our export logistics team utilizes validated thermal shippers to maintain temperature integrity during international transit to Africa, LATAM, and SEA markets.

Accepting B2B inquiries for hospital supply, gastro-specialty tender participation, and global distribution from our Mumbai export hub.

B2B Trade Specifications

Support for Cold-Chain Export?

Yes. We specialize in the logistics of temperature-sensitive injectables. We utilize PCM-based thermal packaging and digital data loggers to ensure that Terlipressin remains within the required 2°C to 8°C range from our Mumbai facility to your final destination.

Registration Assistance Provided?

We provide complete Regulatory Technical Files (CTD), Certificates of Analysis (COA), and stability data to facilitate local health authority approvals and participation in government healthcare or institutional tenders.

Mixed-Container Consolidation?

Through our Mumbai hub, we can consolidate Terlipressin with other gastro/liver care essentials—such as Octreotide, Lactulose, or Albumin—to provide a comprehensive clinical portfolio in a single, cost-effective shipment.

Approx. Rs 24.00 / PieceGet Latest Price

Product Details:

Tranexamic Acid Injection IP 500 Mg (100mg Per Ml)
TRANEXAMIC ACID Injection IP (500 mg / 5 mL)

Healthy Inc offers Tranexamic Acid Injection IP, a high-precision antifibrinolytic agent critical for the control of clinical hemorrhage. Containing 500 mg of Tranexamic Acid in a 5 mL ampoule (100 mg/mL), this formulation is a clinical priority for the treatment and prevention of excessive bleeding in Postpartum Hemorrhage (PPH), major surgery, and trauma. As a specialized Indian export partner, we supply this WHO-essential medicine to maternity hospitals and surgical centers globally.

• Hemostatic Precision: Acts as a potent competitive inhibitor of plasminogen activation. By stabilizing fibrin clots, it prevents their premature dissolution, significantly reducing blood loss and the need for blood transfusions in emergency settings.

• Manufacturing Excellence: Produced in associated WHO-GMP certified sterile facilities. The solution is formulated under strict aseptic conditions to ensure 100% sterility, a controlled physiological pH, and high molecular purity for safe Intravenous (IV) or Intramuscular (IM) administration.

• Clinical Utility: A cornerstone in orthopedic, cardiac, and gynecological surgery. It is increasingly utilized in "Crash" protocols for trauma patients and is the gold standard for managing heavy menstrual bleeding and obstetric hemorrhage.

• Climate Stability: Validated for Zone IVb (Hot/Humid) conditions; vacuum-sealed in USP Type I glass ampoules to maintain chemical integrity and potency during international 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

Logistics & Export Optimization

As a pharmacist-led firm, we understand the critical nature of hemostatic agents. We utilize impact-resistant secondary packaging and offer optimized bulk packing formats that reduce shipping volume, helping you lower freight costs for large-scale institutional tenders.

Registration & Compliance Support

We provide complete Regulatory Technical Files (CTD) and Certificates of Analysis (COA) for every batch. Our documentation is tailored to facilitate rapid health authority approvals and meet the strict requirements of international procurement agencies.

Mixed-Container Consolidation

Through our Mumbai hub, we can consolidate Tranexamic Acid with other surgical and maternal health essentials—such as Oxytocin, Methylergometrine, or Lignocaine—to provide a comprehensive emergency care portfolio in a single, cost-effective shipment.

Direct Sourcing Advantage

Sourced through Healthy Life Group’s associated specialized WHO-GMP units, ensuring competitive direct-from-factory pricing and rigorous quality oversight for high-demand life-saving injectables.

Approx. Rs 1,017.75 / VialGet Latest Price

Product Details:

Meropenem 1000 mg

ZYDOPENEM Injection (Meropenem IP 1 gm)

We are offering ready stock of below brands.Meronem, Meromac, Mero, Merocrit, Merotec, Merobax, Merosure, Merotrol, Meroza, Micropenam, Penmer, Romax, M-Penem, Azopen, Merobik, Redipenem, Neuronem, Meroclip, Gonem, Carbapen M, Cbpenem, Ruaj, Zyonem, Meroreach, Carbonem, Mepecon, Icuber, Nexa, Gerpenem, Zydopenem

Healthy Inc offers ZYDOPENEM, a high-potency carbapenem antibiotic engineered for the treatment of severe, multi-drug resistant (MDR) infections. Containing 1 gm of sterile Meropenem IP, this ultra-broad-spectrum agent is a critical clinical tool in hospital-acquired infections and critical care medicine. As a specialized Indian export partner, we supply this essential anti-infective to Intensive Care Units (ICUs) and surgical centers in global pharmaceutical markets.

• Ultra-Broad Spectrum Efficacy: ZYDOPENEM exhibits potent bactericidal activity by inhibiting cell wall synthesis. It is highly resistant to degradation by most $\beta$-lactamases, including extended-spectrum $\beta$-lactamases (ESBLs), making it effective against a wide range of Gram-positive, Gram-negative, and anaerobic pathogens.

• Clinical Versatility: Indicated for life-threatening conditions such as Septicemia, Nosocomial Pneumonia, complicated Intra-abdominal Infections, and bacterial Meningitis. Its ability to cross the blood-brain barrier makes it a primary choice for CNS infections.

• Manufacturing Excellence: Produced in associated WHO-GMP certified sterile dry-powder facilities. The powder is micronized for rapid, residue-free reconstitution, ensuring 100% molecular purity and a precise pH balance for safe Intravenous (IV) bolus or infusion.

• Climate-Adaptive Stability: Validated for Zone IVb (Hot/Humid) conditions; vacuum-sealed in USP Type I glass vials to maintain potency and prevent degradation during international transit to Africa, LATAM, and SEA markets.

Accepting B2B inquiries for contract manufacturing, bulk supply, and institutional healthcare tender participation from our Mumbai export hub.

B2B Technical Specifications

Logistics & Export Optimization

As a pharmacist-led firm, we understand that sterile powders like ZYDOPENEM are sensitive to moisture and physical shock. We utilize impact-resistant secondary packaging and moisture-sealed cartons to ensure the product reaches your clinical facility in peak condition, maintaining cost-efficiency in freight from Mumbai.

Registration & Compliance Support

We provide complete Regulatory Technical Files (CTD) and batch-wise Certificates of Analysis (COA). Our documentation is specifically designed to facilitate rapid health authority approvals and meet the strict requirements of government healthcare and critical-care tenders.

Approx. Rs 430.00 / PieceGet Latest Price

Product Details:

Cefepime 1Gm + Sulbactum 500Mg Inj

CEFEPIME & SULBACTAM Injection (1.5 gm)

Healthy Inc offers the advanced, synergistic combination of Cefepime & Sulbactam. This formulation pairs a fourth-generation cephalosporin with a potent $\beta$-lactamase inhibitor, specifically engineered to combat life-threatening infections caused by multi-drug resistant (MDR) Gram-negative pathogens. As a specialized Indian export partner, we supply this high-end anti-infective to Intensive Care Units (ICUs), oncology wards, and tertiary care hospitals globally.

• Zwitterionic Penetration & Shielding: Cefepime is a zwitterionic molecule that penetrates the outer membrane of Gram-negative bacteria (via porin channels) at an accelerated rate. By adding Sulbactam, the combination effectively neutralizes bacterial $\beta$-lactamases that would otherwise degrade the antibiotic, restoring activity against resistant Acinetobacter spp., Pseudomonas aeruginosa, and ESBL-producing Enterobacteriaceae.

• Overcoming Resistance Mechanisms: This combination is designed to overcome various resistance mechanisms, including those mediated by plasmid and chromosomal $\beta$-lactamases. It is a critical "reserve" therapeutic for hospital-acquired infections where standard third-generation cephalosporins fail.

• Clinical Criticality: Indicated for the treatment of Febrile Neutropenia, complicated Urinary Tract Infections (UTIs), severe Lower Respiratory Tract Infections (LRTI) including hospital-acquired pneumonia, and complicated intra-abdominal infections.

• Manufacturing Excellence: Produced in associated WHO-GMP certified sterile dry-powder facilities. The formulation often utilizes L-Arginine for pH stabilization, ensuring a clear, residue-free solution for Intravenous (IV) or Intramuscular (IM) administration.

Accepting B2B inquiries for critical care supply, hospital tender participation, and global distribution from our Mumbai export hub.

B2B Trade Specifications

Logistics & Export Optimization

As a pharmacist-led firm, we understand that combinations containing Sulbactam are highly hygroscopic. We utilize moisture-barrier secondary packaging and high-density outer cartons to prevent any "caking" or degradation during international transit to Africa, LATAM, and SEA markets, ensuring the product maintains 100% molecular potency in Zone IVb climates.

Registration & Compliance Support

We provide complete Regulatory Technical Files (CTD) and batch-specific Certificates of Analysis (COA). Our documentation is meticulously structured to meet the high-transparency requirements of private hospital networks and specialized government healthcare tenders.

Approx. Rs 536.95 / VialGet Latest Price

Product Details:

Doxycyline For Injection 100 Mg
LENTECLIN Injection (Doxycycline for Injection USP 100 mg)

Healthy Inc offers LENTECLIN, a high-potency Tetracycline Antibiotic designed for severe systemic infections. Containing Doxycycline Hyclate, it is a clinical priority for treating a broad spectrum of Gram-positive and Gram-negative pathogens, as well as atypical organisms. It is a frontline therapeutic for Severe Respiratory Tract Infections, Rickettsial Infections (Typhus, Spotted Fevers), Cholera, and Lyme Disease, particularly when oral administration is not feasible. As a specialized Indian export partner, we supply this essential anti-infective to infectious disease departments and general hospital networks in global pharmaceutical markets.

• Broad-Spectrum Efficacy: Highly effective against a wide array of pathogens, including those resistant to other antibiotic classes. It is also an essential component in the management of Anthrax and severe Malaria protocols.

• Manufacturing: Produced in associated WHO-GMP certified sterile facilities specialized in Lyophilization (Freeze-Drying), ensuring 100% sterility, high molecular stability, and rapid reconstitution for Intravenous (IV) infusion.

• Climate Stability: Validated for Zone IVb (Hot/Humid) conditions; the lyophilized powder form provides superior resilience to thermal degradation compared to liquid antibiotics, 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 hospital-grade antibiotics.

Accepting B2B inquiries for contract manufacturing, bulk supply, and global distribution partnerships from our Mumbai export hub.

Available strengths and quality? We supply LENTECLIN in vials containing 100 mg of Doxycycline as a sterile lyophilized powder. 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. LENTECLIN is Zone IVb stability-tested. The lyophilized cake is highly stable. We utilize neutral USP Type I glass vials and moisture-resistant secondary packaging to ensure product integrity 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 LENTECLIN with other critical care antibiotics (such as Ceftriaxone, Meropenem, or Azithromycin) 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 250.31 / VialGet Latest Price

Product Details:

Meropenem Injection ( Sodium Carbonate )
MEROBAX 125 mg Injection (Meropenem for Injection USP 125 mg)

Healthy Inc offers MEROBAX 125 mg, a specialized pediatric and low-dose strength of the ultra-broad-spectrum Carbapenem Antibiotic, Meropenem. This dosage is a clinical priority for treating severe infections in neonates, infants, and pediatric patients, as well as for precise dose titration in adult patients with significant renal impairment. It is a frontline therapeutic for Pediatric Meningitis, Neonatal Septicemia, and Complicated Intra-abdominal Infections. As a specialized Indian export partner, we supply this critical anti-infective to neonatal intensive care units (NICU) and pediatric hospitals in global pharmaceutical markets.

• Pediatric Precision: Provides an ideal concentration for neonatal dosing, reducing the risk of medication errors and waste associated with drawing small doses from larger 500 mg or 1 g vials.

• 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 pediatric 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 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 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 pediatric or government hospital tender participations.

Small-volume or mixed orders? We specialize in mixed-container consolidation, allowing you to combine MEROBAX 125 mg with other pediatric 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 50 / PieceGet Latest Price

Product Details:

NITROGLYCERIN (Glyceryl Trinitrate) Injection (5 mg/mL)

Healthy Inc offers Nitroglycerin Injection, a high-precision organic nitrate and potent vasodilator. As a specialized Indian export partner, we supply this critical cardiovascular asset for the acute management of perioperative hypertension and congestive heart failure. Produced in associated WHO-GMP certified sterile facilities, our formulation is a clinical staple in emergency cardiology and surgical suites globally.

• Systemic Vasodilation Mechanism: Nitroglycerin is converted to Nitric Oxide (NO) in the vascular smooth muscle. This activates guanylate cyclase, increasing intracellular cyclic GMP ($cGMP$), which leads to the dephosphorylation of myosin light chains. The result is a profound relaxation of smooth muscle, primarily in the venous system (reducing preload) and, at higher doses, the arterial system (reducing afterload).

• Coronary Hemodynamics: It promotes the redistribution of blood flow toward ischemic areas of the myocardium by dilating large coronary arteries. This reduces myocardial oxygen demand and improves the oxygen supply-demand balance.

• Clinical Criticality: Indicated for the control of Hypertension during cardiac surgery, the treatment of Congestive Heart Failure associated with acute myocardial infarction, and the management of unstable angina unresponsive to conventional therapy.

• Manufacturing Excellence: Our product is a sterile, non-pyrogenic solution. Given that Nitroglycerin can be absorbed by many plastics, we utilize specialized USP Type I Glass Vials/Ampoules to ensure the concentration remains consistent at 5 mg/mL from the factory to the point of care.

B2B Technical Specifications Logistics & Export Optimization

As a pharmacist-led organization, we understand the stability challenges of Nitroglycerin. It is highly light-sensitive and its potency can be compromised if stored in inappropriate containers. We utilize amber glass vials and specialized secondary packaging. Our logistics team ensures that shipments to Africa, LATAM, and SEA are handled with climate-controlled protocols to prevent molecular degradation during transit in Zone IVb environments.

Product Price :Get Latest Price

Product Details:

Ampicillin 250 Mg + Cloxacillin 250 Mg
AMPICILLIN & CLOXACILLIN Injection (250 mg / 500 mg)

Healthy Inc offers the synergistic Ampicillin & Cloxacillin combination (often referred to as Ampiclox). This dual-action antibiotic formulation is a clinical staple, combining a broad-spectrum penicillin with a penicillinase-resistant agent. As a specialized Indian export partner, we supply this essential anti-infective to neonatal units, pediatric wards, and surgical centers globally to combat mixed bacterial infections.

• Broadened Therapeutic Spectrum: While Ampicillin targets a wide range of Gram-positive and Gram-negative bacteria, Cloxacillin specifically neutralizes $\beta$-lactamase-producing Staphylococci. This combination prevents the enzymatic degradation of the antibiotic, making it highly effective against resistant skin, soft tissue, and respiratory infections.

• Clinical Versatility: Widely indicated for Neonatal Sepsis, post-operative wound infections, infected burns, and severe respiratory tract infections. It is a frontline choice in empirical therapy when the specific causative pathogen is yet to be identified.

• Manufacturing Excellence: Produced in associated WHO-GMP certified sterile dry-powder facilities. Both active ingredients are micronized and blended under strict aseptic conditions to ensure rapid, clear reconstitution for Intravenous (IV) or Intramuscular (IM) administration.

• Climate-Adaptive Stability: Validated for Zone IVb (Hot/Humid) conditions. Vacuum-sealed in USP Type I glass vials with high-integrity bungs to maintain 100% molecular potency during international transit to Africa, LATAM, and SEA markets.

Accepting B2B inquiries for high-volume supply, institutional healthcare tenders, and private label manufacturing from our Mumbai export hub.

B2B Trade Specifications

Logistics & Export Optimization

As a pharmacist-led firm, we understand that maintaining the sterility and stability of penicillin combinations is critical. We utilize moisture-barrier secondary packaging and reinforced cartons to ensure the product reaches your facility in peak condition, minimizing the risk of browning or degradation in tropical transit.

Registration & Compliance Support

We provide complete Regulatory Technical Files (CTD) and batch-specific Certificates of Analysis (COA). Our documentation is tailored to meet the requirements of international health authorities, ensuring smooth market entry and successful tender participation.

Approx. Rs 25.59 / 20' ContainerGet Latest Price

Each 10ml Contains: Potassium Chloride B.P. 1.5g, Water For Injection I.P. Q.s.
KCL-CARE (Potassium Chloride Injection IP 15% w/v)

Healthy Inc offers KCL-CARE, a high-concentration Electrolyte Replenisher essential for the management of severe electrolyte imbalances. Containing Potassium Chloride, KCL-CARE is a critical care injectable used to treat and prevent Hypokalemia (low blood potassium levels), especially in patients for whom oral replacement is inadequate or not feasible. It is a clinical priority in ICU and surgical settings for maintaining cardiac function, nerve impulse transmission, and muscle contraction. As a specialized Indian export partner, we supply this life-saving electrolyte solution to hospital networks and emergency care units in global pharmaceutical markets.

• Critical Care Utility: Essential for patients with severe potassium depletion, cardiac arrhythmias due to hypokalemia, or those on prolonged parenteral nutrition.

• Manufacturing: Produced in associated WHO-GMP certified sterile facilities, ensuring 100% sterility, precise concentration (2 mEq of $K^+$ and $Cl^-$ per ml), and strict adherence to Indian Pharmacopoeia (IP) standards.

• Climate Stability: Validated for Zone IVb (Hot/Humid) conditions, ensuring the electrolyte solution 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 of 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 KCL-CARE in the standard 15% w/v concentration, typically available in 10 ml or 20 ml ampoules/vials. Each 10 ml provides approximately 20 mEq of Potassium. Every batch undergoes rigorous assay testing and sterility validation to meet international safety standards.

Safety and Administration?

As a high-alert medication, KCL-CARE is a concentrated solution that must be diluted in a compatible large-volume parenteral fluid (like Normal Saline or Dextrose) before intravenous infusion. Our packaging includes clear "Concentrate: Must be Diluted" warnings to ensure hospital safety compliance.

Support for tropical export?

Yes. KCL-CARE is Zone IVb stability-tested. We utilize neutral USP Type I glass and specialized export-grade secondary packaging to ensure product integrity 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 KCL-CARE with other essential electrolytes (such as Calcium Gluconate or Magnesium Sulfate) 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 electrolyte therapies.