Pharmaceutical Capsules

Approx. Rs 100 / StripGet Latest Price

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METRONIDAZOLE Capsules (500 mg)

Healthy Inc offers Metronidazole Capsules 500 mg, a potent nitroimidazole antibiotic and antiprotozoal. As a pharmacist-led firm, we recognize Metronidazole as an essential "Level 1" antimicrobial in the WHO Model List of Essential Medicines. Managed through our Mumbai export hub, our formulation is produced in associated WHO-GMP certified facilities, ensuring high purity and strict adherence to dissolution profiles for optimal clinical efficacy.

Pharmacological Profile

• Mechanism of Action (DNA Fragmentation): Metronidazole is a prodrug. In anaerobic environments, the nitro group of the molecule is reduced by the microbial protein ferredoxin. This reduction creates highly reactive nitroso free radicals that bind to the microbial DNA, causing strand breakage and helical structure destabilization, which leads to rapid cell death.

• Target Pathogen Spectrum: * Anaerobic Bacteria: Highly effective against Bacteroides fragilis, Clostridium difficile, and Fusobacterium.

  • Protozoa: The gold standard for Entamoeba histolytica (Amoebiasis), Giardia lamblia (Giardiasis), and Trichomonas vaginalis.

• Clinical Indications:

  • Intestinal & Extra-intestinal Amoebiasis: Treatment of liver abscesses and dysentery.

  • Bacterial Vaginosis: A primary therapeutic choice for gynecological infections.

  • H. pylori Eradication: Often utilized as part of "Quadruple Therapy" in regions with high clarithromycin resistance.

  • Surgical Prophylaxis: Used to prevent post-operative anaerobic infections in colorectal and gynecological surgeries.

• Pharmacist’s Clinical Note: Metronidazole is well known for inducing a Disulfiram-like reaction. We emphasize the importance of counseling patients to avoid alcohol during therapy and for at least 48 hours afterward to prevent severe nausea, vomiting, and tachycardia.

B2B Technical Specifications Logistics & Export Optimization

As a pharmacist, you are aware that Metronidazole is relatively stable, but it is photosensitive. Exposure to direct light can lead to the darkening of the active ingredient and a reduction in potency. We utilize opaque capsule shells and high-grade foil packaging as a standard. For our exports to Africa, LATAM, and SEA, our Mumbai logistics team ensures that shipments are protected from extreme thermal fluctuations in Zone IVb climates to prevent any physical degradation of the capsule shell.

Approx. Rs 306.59 / PieceGet Latest Price

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CADFOL-S Injection (Iron Sucrose Injection USP)

Healthy Inc offers high-quality CADFOL-S, containing Iron Sucrose, a critical intravenous iron replacement therapy. It is specifically formulated for the treatment of iron deficiency anemia in patients with chronic kidney disease (CKD) or those who cannot tolerate oral iron therapy. Our Monocarton with Tray Pack packaging ensures maximum ampoule protection and professional presentation for clinical environments. As a leading Indian export partner, we provide high-purity hematinic solutions for global pharmaceutical markets.

• Manufacturing: Produced in associated WHO-GMP certified sterile facilities adhering to USP and international pharmacopoeia standards for guaranteed safety and high elemental iron bioavailability.

• Climate Stability: Validated for Zone IVb (Hot/Humid) conditions, ensuring molecular stability of the iron-sucrose complex across Africa, LATAM, and SEA markets.

• Regulatory Support: Full technical documentation available, including CTD/eCTD Dossiers to streamline the registration process for essential hematinic medications.

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

Available strengths and quality? We supply CADFOL-S in the standard 20 mg elemental iron per ml concentration (typically 5ml ampoules providing 100 mg iron). Every batch undergoes rigorous sterility, pH, and molecular weight distribution testing to meet global purity standards.

Packaging Specification? This product is supplied in a Monocarton with Tray Pack. The plastic tray prevents ampoule breakage during international transit, while the monocarton provides a professional, retail-ready finish for hospitals and pharmacies.

Support for tropical export? Yes. All formulations are Zone IVb stability-tested to prevent precipitation or chemical degradation in high-temperature and high-humidity regions, ensuring a long shelf life for international transit.

Registration assistance provided? We provide complete Regulatory Technical Files (CTD) to facilitate local import licensing and health authority approvals in your specific international region.

Small-volume or mixed orders? We specialize in mixed-container consolidation, allowing you to combine hematinics with other therapeutic categories (like anesthesia or antibiotics) in a single, cost-effective shipment.

Direct manufacturing? Products are sourced through Healthy Life Group’s associated WHO-GMP manufacturing units, ensuring direct-from-factory pricing and strict quality control oversight.

Approx. Rs 66.62 / VialGet Latest Price

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ceftriaxone 1000 mg
CADICEFT 1G Injection (Ceftriaxone for Injection IP 1 GM)

Healthy Inc offers high-quality CADICEFT 1G, containing Ceftriaxone, a premier Third-Generation Cephalosporin Antibiotic. This broad-spectrum injectable is a clinical mainstay for treating severe bacterial infections, including lower respiratory tract infections, pelvic inflammatory disease, bacterial septicemia, and bone/joint infections. As a dedicated Indian export hub, we provide high-purity anti-infective solutions for hospital networks in global pharmaceutical markets.

• Manufacturing: Produced in associated WHO-GMP certified sterile facilities adhering to Indian Pharmacopoeia (IP) and international quality standards for guaranteed safety and high efficacy.

• Climate Stability: Validated for Zone IVb (Hot/Humid) conditions, ensuring therapeutic potency and molecular stability across Africa, LATAM, and SEA markets.

• Regulatory Support: Full technical documentation available, including CTD/eCTD Dossiers to streamline the registration process for essential antibiotic therapies.

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

Available strengths and quality? We supply CADICEFT 1G as a sterile powder for injection in a 1x1 Vial configuration (Single vial with tray/monocarton). Every batch undergoes rigorous sterility, bacterial endotoxin, and potency testing to meet global purity standards.

What does "SL DOM" signify? This refers to the specific packaging and labeling standards often utilized for Domestic/Selected Market supply chains, ensuring compliance with local regulatory identification while maintaining international manufacturing quality.

Support for tropical export? Yes. All formulations are Zone IVb stability-tested to prevent chemical degradation in high-temperature and high-humidity regions, ensuring a long shelf life for international transit.

Registration assistance provided? We provide complete Regulatory Technical Files (CTD) to facilitate local import licensing and health authority approvals in your specific international region.

Small-volume or mixed orders? We specialize in mixed-container consolidation, allowing you to combine Ceftriaxone with other therapeutic categories (such as anesthesia or nutritional injectables) 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 direct-from-factory pricing and strict quality control oversight.

Approx. Rs 66.62 / VialGet Latest Price

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ceftriaxone 1000 mg
CADICEFT 1GM Injection (Ceftriaxone for Injection IP 1 GM)

Healthy Inc offers high-quality CADICEFT 1GM, featuring Ceftriaxone, a cornerstone Third-Generation Cephalosporin Antibiotic. This broad-spectrum injectable is a critical clinical tool for treating severe bacterial infections, including meningitis, pneumonia, abdominal infections, and for surgical prophylaxis. As a specialized Indian export partner, we provide high-purity anti-infective solutions for hospital networks and emergency care in global pharmaceutical markets.

• Manufacturing: Produced in associated WHO-GMP certified sterile facilities adhering to Indian Pharmacopoeia (IP) and international standards for guaranteed safety and clinical efficacy.

• Climate Stability: Validated for Zone IVb (Hot/Humid) conditions, ensuring therapeutic potency and molecular stability across Africa, LATAM, and SEA markets.

• Regulatory Support: Full technical documentation available, including CTD/eCTD Dossiers to streamline the registration process for essential antibiotic medications.

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

Available strengths and quality? We supply CADICEFT 1GM as a sterile powder for injection in vials. Every batch undergoes rigorous sterility, bacterial endotoxin, and potency testing to meet global purity standards and consistent clinical performance.

Support for tropical export? Yes. All formulations are Zone IVb stability-tested to prevent chemical degradation in high-temperature and high-humidity regions, ensuring a long shelf life for international transit.

Registration assistance provided? We provide complete Regulatory Technical Files (CTD) to facilitate local import licensing and health authority approvals in your specific international region.

Small-volume or mixed orders? We specialize in mixed-container consolidation, allowing you to combine Ceftriaxone with other therapeutic categories 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 direct-from-factory pricing and strict quality control oversight.

Approx. Rs 43.13 / PieceGet Latest Price

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Cefoperazone Injection IP 1 G
Cefoperazone Injection IP 1g (Sterile Cefoperazone Sodium)

Healthy Inc offers high-quality Cefoperazone 1g, a potent Third-Generation Cephalosporin Antibiotic. It is widely recognized for its superior activity against Pseudomonas aeruginosa and other Gram-negative aerobic bacteria. This injectable is a clinical mainstay for treating biliary tract infections, respiratory infections, and peritonitis due to its unique biliary excretion profile. As a specialized Indian export partner, we provide high-purity anti-infective solutions for hospital networks in global pharmaceutical markets.

• Manufacturing: Produced in associated WHO-GMP certified sterile facilities adhering to Indian Pharmacopoeia (IP) and international standards for guaranteed safety and clinical efficacy.

• Climate Stability: Validated for Zone IVb (Hot/Humid) conditions, ensuring therapeutic potency and molecular stability across Africa, LATAM, and SEA markets.

• Regulatory Support: Full technical documentation available, including CTD/eCTD Dossiers to streamline the registration process for essential antibiotic therapies.

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

Available strengths and quality? We supply Cefoperazone 1g as a sterile powder for injection in vials. Every batch undergoes rigorous sterility, bacterial endotoxin, and potency testing to meet global purity standards and ensure consistent clinical performance.

Support for tropical export? Yes. All formulations are Zone IVb stability-tested to prevent chemical degradation in high-temperature and high-humidity regions, ensuring a long shelf life for international transit.

Registration assistance provided? We provide complete Regulatory Technical Files (CTD) to facilitate local import licensing and health authority approvals in your specific international region.

Small-volume or mixed orders? We specialize in mixed-container consolidation, allowing you to combine Cefoperazone with other therapeutic categories (such as anesthesia or nutritional injectables) 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 direct-from-factory pricing and strict quality control oversight.

Approx. Rs 9.38 / PieceGet Latest Price

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Cefotaxime Sodium Injection IP 250 Mg
Cefotaxime Sodium Injection IP 250 mg (Pediatric Strength)

Healthy Inc offers high-quality Cefotaxime 250 mg, a vital Third-Generation Cephalosporin Antibiotic in a specialized pediatric strength. It provides broad-spectrum coverage against Gram-positive and Gram-negative pathogens and is a clinical priority for neonatal and pediatric care, particularly in treating meningitis, respiratory infections, and early-stage sepsis. As a leading Indian export partner, we provide high-purity anti-infective solutions for neonatal intensive care units (NICU) and pediatric wards in global pharmaceutical markets.

• Manufacturing: Produced in associated WHO-GMP certified sterile facilities adhering to Indian Pharmacopoeia (IP) and international quality standards for guaranteed safety and precision dosing.

• Climate Stability: Validated for Zone IVb (Hot/Humid) conditions, ensuring therapeutic potency and molecular stability across Africa, LATAM, and SEA markets.

• Regulatory Support: Full technical documentation available, including CTD/eCTD Dossiers to streamline the registration process for essential life-saving antibiotics.

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

Available strengths and quality? We supply Cefotaxime 250 mg as a sterile powder for injection in vials. Every batch undergoes rigorous sterility, bacterial endotoxin, and HPLC-based potency testing to meet global purity standards and ensure safe administration in sensitive pediatric populations.

Support for tropical export? Yes. All formulations are Zone IVb stability-tested to prevent chemical degradation in high-temperature and high-humidity regions, ensuring a long shelf life for international transit.

Registration assistance provided? We provide complete Regulatory Technical Files (CTD) to facilitate local import licensing and health authority approvals in your specific international region.

Small-volume or mixed orders? We specialize in mixed-container consolidation, allowing you to combine pediatric-strength antibiotics with other therapeutic categories (such as nutritional injectables or anti-emetics) 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 direct-from-factory pricing and strict quality control oversight.

Approx. Rs 42.66 / PieceGet Latest Price

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Approx. Rs 75.00 / VialGet Latest Price

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Ceftazidime Injection IP 1g
Ceftazidime Injection IP 1g (Sterile Ceftazidime Sodium)

Healthy Inc offers high-purity Ceftazidime 1g, a definitive Third-Generation Cephalosporin Antibiotic known for its exceptional activity against Pseudomonas aeruginosa. Unlike other cephalosporins, Ceftazidime is highly resistant to most beta-lactamases, making it a frontline choice for hospital-acquired infections, including nosocomial pneumonia, complicated urinary tract infections, and infections in immunocompromised patients. As a specialized Indian export partner, we provide high-purity anti-infective solutions for critical care and ICU settings in global pharmaceutical markets.

• Manufacturing: Produced in associated WHO-GMP certified sterile facilities adhering to Indian Pharmacopoeia (IP) and international standards for guaranteed safety, high molecular purity, and clinical efficacy.

• Climate Stability: Validated for Zone IVb (Hot/Humid) conditions, ensuring therapeutic potency and powder stability across Africa, LATAM, and SEA markets.

• Regulatory Support: Full technical documentation available, including CTD/eCTD Dossiers to streamline the registration process for essential anti-pseudomonal therapies.

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

Available strengths and quality? We supply Ceftazidime 1g as a sterile powder for injection in vials. Every batch undergoes rigorous sterility, bacterial endotoxin, and HPLC-based potency testing to meet global purity standards and ensure consistent clinical performance in high-stakes environments.

Support for tropical export? Yes. All formulations are Zone IVb stability-tested to prevent chemical degradation in high-temperature and high-humidity regions, ensuring a long shelf life for international transit.

Registration assistance provided? We provide complete Regulatory Technical Files (CTD) to facilitate local import licensing and health authority approvals in your specific international region.

Small-volume or mixed orders? We specialize in mixed-container consolidation, allowing you to combine Ceftazidime with other therapeutic categories (such as anesthesia, anti-emetics, or GI care) 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 direct-from-factory pricing and strict quality control oversight.

Approx. Rs 46.88 / VialGet Latest Price

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Ceftazidime Injection IP 500mg
Ceftazidime Injection IP 500 mg (Sterile Ceftazidime Sodium)

Healthy Inc offers high-quality Ceftazidime 500 mg, a potent Third-Generation Cephalosporin Antibiotic. This strength is widely utilized for both pediatric dosing and moderate infections in adult patients, providing exceptional bactericidal activity against Pseudomonas aeruginosa and other Gram-negative aerobic bacteria. It is a clinical staple for treating lower respiratory tract infections, skin and skin structure infections, and complicated urinary tract infections where resistance to other cephalosporins is suspected. As a specialized Indian export partner, we provide high-purity anti-infective solutions for hospital networks and clinics in global pharmaceutical markets.

• Manufacturing: Produced in associated WHO-GMP certified sterile facilities adhering to Indian Pharmacopoeia (IP) and international quality standards for guaranteed safety, sterility, and therapeutic precision.

• Climate Stability: Validated for Zone IVb (Hot/Humid) conditions, ensuring therapeutic potency and molecular stability across Africa, LATAM, and SEA markets.

• Regulatory Support: Full technical documentation available, including CTD/eCTD Dossiers to streamline the registration process for essential antibiotic therapies.

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

Available strengths and quality? We supply Ceftazidime 500 mg as a sterile powder for injection in vials. Every batch undergoes rigorous sterility, bacterial endotoxin, and HPLC-based potency testing to meet global purity standards and ensure consistent clinical performance.

Support for tropical export? Yes. All formulations are Zone IVb stability-tested to prevent chemical degradation in high-temperature and high-humidity regions, ensuring a long shelf life for international transit.

Registration assistance provided? We provide complete Regulatory Technical Files (CTD) to facilitate local import licensing and health authority approvals in your specific international region.

Small-volume or mixed orders? We specialize in mixed-container consolidation, allowing you to combine this antibiotic with other therapeutic categories (such as anesthesia, anti-emetics, or GI care) 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 direct-from-factory pricing and strict quality control oversight.

Approx. Rs 65.63 / VialGet Latest Price

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Cefuroxime Injection IP 1500mg
Cefuroxime Injection IP 1500mg (Sterile Cefuroxime Sodium)

Healthy Inc offers high-potency Cefuroxime 1500mg (1.5g), a definitive Second-Generation Cephalosporin Antibiotic. Cefuroxime is distinguished by its high stability against many bacterial beta-lactamases and its broad-spectrum activity against both Gram-positive and Gram-negative organisms. This 1500mg dosage is a clinical standard for surgical prophylaxis—significantly reducing post-operative infection rates—and for treating severe respiratory infections and bone/joint infections. As a specialized Indian export partner, we provide high-purity anti-infective solutions for surgical units and hospital networks in global pharmaceutical markets.

• Manufacturing: Produced in associated WHO-GMP certified sterile facilities adhering to Indian Pharmacopoeia (IP) and international standards for 100% sterility and high molecular purity.

• Climate Stability: Validated for Zone IVb (Hot/Humid) conditions, ensuring therapeutic potency and powder stability across Africa, LATAM, and SEA markets.

• Regulatory Support: Full technical documentation available, including CTD/eCTD Dossiers to streamline the registration process for essential antibiotic therapies.

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

Available strengths and quality? We supply Cefuroxime 1500mg as a sterile powder for injection in vials. Every batch undergoes rigorous sterility testing, bacterial endotoxin limits (BET), and HPLC-based potency assays to meet global purity standards and ensure consistent clinical performance.

Support for tropical export? Yes. All formulations are Zone IVb stability-tested to prevent chemical degradation in high-temperature and high-humidity regions, ensuring a long shelf life for international transit and storage.

Registration assistance provided? We provide complete Regulatory Technical Files (CTD) and Certificates of Analysis (COA) to facilitate local import licensing and health authority approvals in your specific international region.

Small-volume or mixed orders? We specialize in mixed-container consolidation, allowing you to combine Cefuroxime with other therapeutic categories (such as anesthesia, anti-emetics, or other cephalosporins) 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 261.42 / PieceGet Latest Price

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artesunate 60 mg + sodium bicarbonate 5% w/v + sodium chloride 0.9% w/v
CHINSUNATE Injection (Artesunate Injection 60 mg/1 ml)

Healthy Inc offers CHINSUNATE, a life-saving antimalarial injectable containing Artesunate. It is the WHO-recommended frontline treatment for Severe Malaria caused by Plasmodium falciparum in both adults and children. CHINSUNATE provides rapid clearance of parasitemia and is critical for reducing mortality in complicated malaria cases where oral medication is not feasible. As a specialized Indian export partner, we provide this essential emergency medicine to hospital networks and health ministries across high-burden malaria regions.

• Manufacturing: Produced in associated WHO-GMP certified sterile facilities adhering to international pharmacopoeia standards for guaranteed sterility, high molecular purity, and rapid therapeutic onset.

• Climate Stability: Validated for Zone IVb (Hot/Humid) conditions, ensuring that the active artesunate 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 antimalarial therapies.

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

Available strengths and quality? We supply CHINSUNATE as a sterile powder for injection (60 mg) accompanied by the required ampoules of Sodium Bicarbonate and Sodium Chloride for reconstitution. Every batch undergoes rigorous HPLC-based assay testing and bacterial endotoxin testing (BET) to ensure safety and clinical efficacy.

Support for tropical export? Yes. Since Artesunate is heat-sensitive, our CHINSUNATE is Zone IVb stability-tested. We use specialized export-grade secondary packaging to ensure the product's integrity is maintained during international transit to tropical regions.

Registration assistance provided? We provide complete Regulatory Technical Files (CTD) and Certificates of Analysis (COA) to facilitate local health authority approvals and tender participations in your specific region.

Small-volume or mixed orders? We specialize in mixed-container consolidation, allowing you to combine CHINSUNATE with other essential medicines (such as antibiotics, IV fluids, or critical care injectables) 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 32.82 / VialGet Latest Price

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Cisplatin Injection IP 10 Mg Per10ml
Cisplatin Injection IP 10 mg per 10 ml (1 mg/ml Concentration)

Healthy Inc offers high-purity Cisplatin 10 mg, a fundamental Platinum-based Antineoplastic agent essential for systemic chemotherapy. As a potent cytotoxic agent, Cisplatin induces DNA cross-linking to inhibit the replication of malignant cells. This 10 mg presentation is widely utilized for precision dosing in combination chemotherapy regimens and pediatric oncology. It is a clinical cornerstone for treating metastatic testicular tumors, metastatic ovarian tumors, and advanced bladder cancer. As a specialized Indian export partner, we provide high-quality oncology solutions for specialized cancer centers and hospital networks in global pharmaceutical markets.

• Manufacturing: Produced in associated WHO-GMP certified specialized oncology facilities, adhering to Indian Pharmacopoeia (IP) and international standards for sterile liquid injectables to ensure maximum purity and precision.

• Climate Stability: Validated for Zone IVb (Hot/Humid) conditions, ensuring molecular stability and potency across Africa, LATAM, and SEA markets.

• Regulatory Support: Full technical documentation available, including CTD/eCTD Dossiers to streamline the registration process for essential cytotoxic therapies.

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

Available strengths and quality? We supply Cisplatin as a sterile aqueous solution in 10 mg/10 ml vials. Every batch undergoes rigorous HPLC-based assay testing, sterility validation, and bacterial endotoxin testing (BET) to meet international pharmacopoeia standards for cytotoxic medications.

Support for tropical export? Yes. Our oncology range is Zone IVb stability-tested. We utilize specialized light-resistant packaging protocols to ensure the integrity of the platinum complex during international transit to tropical regions.

Registration assistance provided? We provide complete Regulatory Technical Files (CTD) and Certificates of Analysis (COA) to facilitate local health authority approvals and oncology-specific import licensing in your specific country.

Small-volume or mixed orders? We specialize in mixed-container consolidation, allowing you to combine Cisplatin with other oncology agents, anti-emetics, or critical care injectables in a single, cost-effective shipment to optimize your hospital inventory.

Direct manufacturing? Products are sourced through Healthy Life Group’s associated WHO-GMP manufacturing units, ensuring competitive direct-from-factory pricing and stringent quality control oversight.

Approx. Rs 18.75 / BoxGet Latest Price

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Dextrose 5%w/v And Sodium Chloride 0.9%w/v Injection IP
Dextrose 5% w/v and Sodium Chloride 0.9% w/v Injection IP (DNS)

Healthy Inc offers Dextrose 5% and Sodium Chloride 0.9%, a sterile, non-pyrogenic Isotonic Rehydration solution. Commonly referred to as DNS, this intravenous fluid is a clinical essential for the simultaneous restoration of fluid volume, electrolyte balance (sodium and chloride), and caloric intake. It is the primary choice for managing Dehydration, Heat Exhaustion, and providing Post-operative Fluid Maintenance. As a specialized Indian export partner, we provide these foundational IV solutions to hospital networks and emergency clinics in global pharmaceutical markets.

• Manufacturing: Produced in associated WHO-GMP certified large-volume parenteral (LVP) facilities using advanced BFS (Blow-Fill-Seal) technology to ensure 100% sterility and a particle-free solution.

• Climate Stability: Validated for Zone IVb (Hot/Humid) conditions, ensuring the dextrose remains stable and the container integrity is maintained across Africa, LATAM, and SEA markets.

• Regulatory Support: Full technical documentation available, including CTD Dossiers, to streamline the registration process for essential IV fluids in international territories.

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

Available packaging and quality? We supply this injection in 500 ml and 1000 ml medical-grade LDPE/PP bottles (BFS technology). Every batch undergoes rigorous assay testing for Dextrose and NaCl, sterility validation, and Bacterial Endotoxin Testing (BET) to meet Indian Pharmacopoeia (IP) and international standards.

Support for tropical export? Yes. Our IV fluids are Zone IVb stability-tested. The BFS containers are designed to withstand the pressures of international transit and remain chemically stable in high-temperature and high-humidity environments.

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 container consolidation, allowing you to combine DNS with other IV fluids (such as Normal Saline or Ringer's Lactate) and injectable 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 for large-volume parenterals.

Approx. Rs 5.42 / PieceGet Latest Price

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diclofenac sodium 25 mg
DICLOKEM Injection (Diclofenac Sodium 75 mg / 3 ml)

Healthy Inc offers DICLOKEM, a high-potency Non-Steroidal Anti-Inflammatory Drug (NSAID) and fast-acting analgesic. Containing Diclofenac Sodium, DICLOKEM is a clinical priority for the rapid relief of acute, severe pain and inflammation. It is a frontline therapeutic for the management of Renal Colic, Biliary Colic, Post-operative Pain, and acute exacerbations of Rheumatoid Arthritis or Osteoarthritis. As a specialized Indian export partner, we supply this essential pain management solution to emergency departments and surgical clinics in global pharmaceutical markets.

• Manufacturing: Produced in associated WHO-GMP certified sterile facilities, ensuring 100% sterility, high molecular purity, and precise formulation stability for deep Intramuscular (IM) or slow Intravenous (IV) administration.

• Climate Stability: Validated for Zone IVb (Hot/Humid) conditions, ensuring therapeutic potency and preventing the crystallization of the active ingredient across Africa, LATAM, and SEA markets.

• Regulatory Support: Full technical documentation available, including CTD/eCTD Dossiers to streamline the registration process for essential analgesic injectables.

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

Available strengths and quality? We supply DICLOKEM in 3 ml ampoules containing 75 mg of Diclofenac Sodium (25 mg/ml). Every batch undergoes rigorous HPLC-based assay testing, sterility validation, and pH stability checks to meet international pharmacopoeia standards.

Support for tropical export? Yes. DICLOKEM 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 hospital tender participations in your specific region.

Small-volume or mixed orders? We specialize in mixed-container consolidation, allowing you to combine DICLOKEM with other therapeutic categories (such as antispasmodics like COLIKEM-D, antibiotics, or PPI injectables) 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 2,531.25 / VialGet Latest Price

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Docetaxel Injection IP 120 Mg

Docetaxel Injection IP 120 mg (Cytotoxic Antineoplastic Agent)

Healthy Inc offers Docetaxel 120 mg, a high-potency Taxane antineoplastic agent essential for advanced oncology protocols. Docetaxel works by promoting the assembly of tubulin into stable microtubules and inhibiting their disassembly, which leads to cell cycle arrest and apoptosis of malignant cells. It is a clinical cornerstone for the treatment of Breast Cancer, Non-Small Cell Lung Cancer (NSCLC), Prostate Cancer, Gastric Adenocarcinoma, and Head and Neck Cancer. As a specialized Indian export partner, we provide these high-criticality oncology solutions to cancer institutes and hospital networks in global pharmaceutical markets.

• Manufacturing: Produced in associated WHO-GMP certified oncology-dedicated facilities, ensuring 100% sterility, precise concentration, and zero cross-contamination in accordance with Indian Pharmacopoeia (IP) standards.

• Climate Stability: Validated for Zone IVb (Hot/Humid) conditions; the formulation is stabilized with a specialized solvent system to maintain chemical integrity and prevent precipitation 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 Docetaxel as a sterile concentrated solution in vials containing 120 mg. Every batch undergoes rigorous HPLC-based assay testing, sterility validation, and bacterial endotoxin testing (BET) to ensure the highest safety profile for intravenous infusion.

Support for tropical export? Yes. Docetaxel is sensitive to temperature fluctuations. Our product is Zone IVb stability-tested, utilizing specialized medical-grade primary packaging and secondary insulation to ensure the molecule remains stable during international transit to tropical 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 Docetaxel 120 mg with other oncology agents (such as Paclitaxel or Cyclophosphamide), 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 drug handling.

Approx. Rs 215.63 / PieceGet Latest Price

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Erythropoietin Injection IP 2000 IU
Erythropoietin Injection IP 2000 IU (Recombinant Human Erythropoietin)

Healthy Inc offers Erythropoietin (EPO) 2000 IU, a high-precision Erythropoiesis-Stimulating Agent (ESA). Produced via recombinant DNA technology, this injectable is a clinical cornerstone for the treatment of Anemia associated with Chronic Kidney Disease (CKD), patients on dialysis, and anemia induced by chemotherapy in cancer patients. It effectively stimulates the bone marrow to produce red blood cells, reducing the need for blood transfusions. As a specialized Indian export partner, we supply this essential biological to nephrology clinics and oncology centers in global pharmaceutical markets.

• Precision Biological: Formulated as Epoetin Alfa or Beta, ensuring high biological activity and consistent hemoglobin response via Subcutaneous (SC) or Intravenous (IV) administration.

• Manufacturing: Produced in associated WHO-GMP certified specialized biotech facilities, ensuring 100% sterility, viral safety, and strict adherence to Indian Pharmacopoeia (IP) standards for recombinant proteins.

• Cold Chain Integrity: Validated for strict 2°C to 8°C storage; we utilize advanced thermal packaging and validated cold-chain logistics to maintain protein stability during international transit.

• Regulatory Support: Full technical documentation available, including CTD/eCTD Dossiers and biological characterization data, to streamline registration in international territories.

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

Available strengths and packaging? We supply Erythropoietin in Pre-Filled Syringes (PFS) or vials in the 2000 IU strength. Other concentrations (4000 IU, 10000 IU) are also available to meet diverse clinical requirements for dosage titration.

Support for international shipping? Yes. Being a biological product, we utilize validated cold-chain shipping solutions. Our packaging is designed to maintain the required 2°C to 8°C temperature range throughout transit to Africa, LATAM, and SEA markets, ensuring the protein does not denature.

Registration assistance provided? We provide complete Regulatory Technical Files (CTD), Certificates of Analysis (COA), and Batch Release Certificates to facilitate local health authority approvals and hospital tender participations.

Small-volume or mixed orders? We specialize in consolidated shipments, allowing you to combine Erythropoietin with other nephrology or oncology products (such as Iron Sucrose or Heparin) in a single, temperature-controlled, cost-effective shipment.

Direct sourcing? Products are sourced through Healthy Life Group’s associated WHO-GMP specialized biotech units, ensuring competitive direct-from-factory pricing and rigorous quality control for biosimilar products.

Approx. Rs 4,200.00 / VialGet Latest Price

Product Details:

Approx. Rs 37.50 / BoxGet Latest Price

Product Details:

Folic Acid 15mg, Cyanocobalamine 500mcg And Nicotinamide 200mg Injection
Folic Acid, Cyanocobalamin, and Nicotinamide Injection (High-Potency Vitamin B Complex)

Healthy Inc offers this high-potency Multivitamin (B-Complex) combination, a clinical priority for the rapid correction of severe nutritional deficiencies and neurological support. This synergistic formulation contains Folic Acid (Vitamin B9), Cyanocobalamin (Vitamin B12), and Nicotinamide (Vitamin B3). It is the frontline therapeutic for Megaloblastic Anemia, Peripheral Neuropathy, Alcoholic Neuropathy, and as a critical recovery supplement in cases of Malabsorption Syndrome or chronic exhaustion. As a specialized Indian export partner, we supply these essential vitamins to clinical networks and geriatric care centers in global pharmaceutical markets.

• Clinical Utility: Designed to restore neurological health and hematopoietic function. Folic Acid and B12 are essential for DNA synthesis and RBC maturation, while Nicotinamide supports cellular metabolism and skin integrity.

• Manufacturing: Produced in associated WHO-GMP certified sterile facilities, ensuring 100% sterility, high molecular purity, and precise ratio accuracy for Intramuscular (IM) or Intravenous (IV) administration.

• Climate Stability: Validated for Zone IVb (Hot/Humid) conditions, ensuring the vitamins 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 vials or ampoules containing 15 mg Folic Acid, 500 mcg Cyanocobalamin, and 200 mg Nicotinamide. Every batch undergoes rigorous HPLC-based assay testing and sterility validation to meet international pharmacopoeia standards.

Support for tropical export? Yes. B-Vitamins are sensitive to light and heat. Our formulation is Zone IVb stability-tested, utilizing amber USP Type I glass and specialized light-protective secondary packaging to prevent vitamin degradation 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 hospital tender participations in your specific territory.

Small-volume or mixed orders? We specialize in mixed-container consolidation, allowing you to combine these vitamin injectables with other therapeutic categories (such as Iron Sucrose, Antibiotics, or Analgesics) 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 for essential nutritional therapies.

Approx. Rs 225.00 / VialGet Latest Price

Product Details:

Gemcitabine Injection IP 200mg
Gemcitabine for Injection IP 200 mg (Cytotoxic Antineoplastic Agent)

Healthy Inc offers Gemcitabine 200 mg, a high-precision Pyrimidine Nucleoside Antimetabolite used in the treatment of diverse solid tumors. Gemcitabine acts by inhibiting DNA synthesis, specifically disrupting the S-phase of the cell cycle. It is a clinical priority for the management of Metastatic Pancreatic Cancer, Non-Small Cell Lung Cancer (NSCLC), Bladder Cancer, and Advanced Breast and Ovarian Cancers. As a specialized Indian export partner, we supply these high-criticality oncology solutions to specialized cancer institutes and oncology networks in global pharmaceutical markets.

• Superior Stability: Supplied as a Lyophilized (Freeze-Dried) Powder to ensure maximum molecular stability and rapid reconstitution for Intravenous (IV) infusion.

• 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 lyophilized formulation ensures the chemical integrity of the active pharmaceutical ingredient across Africa, LATAM, and SEA markets.

• Regulatory Support: Full technical documentation available, including CTD/eCTD Dossiers and specialized safety data sheets (MSDS), 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 Gemcitabine in vials containing 200 mg of lyophilized powder, which is ideal for precise dose titration. We also offer 1000 mg (1 g) presentations for higher dose requirements. Every batch undergoes rigorous HPLC-based assay testing, sterility validation, and Bacterial Endotoxin Testing (BET).

Support for tropical export? Yes. Lyophilized Gemcitabine is highly resilient to thermal fluctuations. It is Zone IVb stability-tested, utilizing neutral USP Type I glass vials and specialized export-grade 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 oncology hospital tender participations in your specific territory.

Small-volume or mixed orders? We specialize in mixed-container consolidation, allowing you to combine Gemcitabine with other oncology agents (such as Paclitaxel, Cisplatin, or Etoposide) and supportive care injectables in a single, cost-effective shipment.

Direct sourcing? Products are sourced through Healthy Life Group’s associated WHO-GMP specialized oncology manufacturing units, ensuring competitive direct-from-factory pricing and strict quality control oversight for high-potency antineoplastic therapies.

Approx. Rs 6.57 / VialGet Latest Price

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Glycopyrrolate Injection IP 0.2mg
Glycopyrrolate Injection IP (0.2 mg / ml)

Healthy Inc offers Glycopyrrolate 0.2 mg, a high-precision Anticholinergic (Antimuscarinic) agent. As a quaternary ammonium compound, Glycopyrrolate does not cross the blood-brain barrier, providing targeted peripheral action with minimal central nervous system effects. It is a clinical priority in Anesthesiology and Critical Care for the reduction of salivary, tracheobronchial, and pharyngeal secretions. It is a frontline therapeutic for Pre-operative medication, the reversal of neuromuscular blockade, and the management of Peptic Ulcers. As a specialized Indian export partner, we supply this essential anesthetic adjunct to surgical centers and ICU networks in global pharmaceutical markets.

• Targeted Clinical Profile: Offers superior control of secretions with a lower incidence of tachycardia compared to Atropine, making it ideal for cardiovascularly sensitive patients during surgery.

• Manufacturing: Produced in associated WHO-GMP certified sterile facilities, ensuring 100% sterility, high molecular purity, and precise 0.2 mg/ml concentration for Intramuscular (IM) or Intravenous (IV) 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 of essential anesthetic injectables in international territories.

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

Available strengths and quality? We supply Glycopyrrolate in 1 ml or 2 ml ampoules containing 0.2 mg per ml. Every batch undergoes rigorous HPLC-based assay testing, sterility validation, and pH stability checks to meet Indian Pharmacopoeia (IP) and international standards.

Support for tropical export? Yes. Our Glycopyrrolate 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 government hospital tender participations in your specific region.

Small-volume or mixed orders? We specialize in mixed-container consolidation, allowing you to combine Glycopyrrolate with other anesthetic adjuncts (such as Neostigmine, Atracurium, or Midazolam) in a single, cost-effective shipment to optimize your inventory.

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 critical care therapies.

Approx. Rs 20.63 / VialGet Latest Price

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Lignocaine And Adrenaline Injection IP (2%w/v And 1:80000)
Lignocaine and Adrenaline Injection IP (2% w/v and 1:80,000)

Healthy Inc offers the combination of Lignocaine (Lidocaine) and Adrenaline (Epinephrine), a high-precision Local Anesthetic with Vasoconstrictor. Lignocaine provides rapid-onset nerve blockade by inhibiting sodium channels, while the addition of Adrenaline at a 1:80,000 ratio induces localized vasoconstriction. This clinical priority serves to prolong the duration of anesthesia, reduce localized bleeding (hemostasis) at the surgical site, and decrease the systemic absorption rate of the anesthetic. As a specialized Indian export partner, we supply this essential agent to dental clinics, surgical units, and emergency departments in global pharmaceutical markets.

• Clinical Utility: Primary choice for local infiltration, minor surgical procedures, and dental anesthesia where a bloodless field and extended duration of action are required.

• Manufacturing: Produced in associated WHO-GMP certified sterile facilities, ensuring 100% sterility, precise pH balance, and accurate dilution of the vasoconstrictor component.

• Climate Stability: Validated for Zone IVb (Hot/Humid) conditions; the formulation is stabilized to prevent the 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 strengths and packaging? We supply this combination in 30 ml and 50 ml multi-dose vials, as well as 2 ml ampoules. The formulation contains 20 mg of Lignocaine Hydrochloride per ml with Adrenaline Bitartrate (1:80,000). Every batch undergoes rigorous HPLC-based assay testing and sterility validation to meet Indian Pharmacopoeia (IP) standards.

Support for tropical export? Yes. Adrenaline is naturally light and heat-sensitive; however, our product is Zone IVb stability-tested. We utilize neutral USP Type I amber glass vials and specialized export-grade secondary packaging to protect the molecule from oxidation and light degradation 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/surgical tender participations in your specific territory.

Small-volume or mixed orders? We specialize in mixed-container consolidation, allowing you to combine Lignocaine and Adrenaline with other surgical essentials (such as Bupivacaine, Ketorolac, or sterile 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 pain management and anesthetic therapies.

Approx. Rs 28.13 / VialGet Latest Price

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Nandrolone Decanoate Injection IP 50mg/ml
Nandrolone Decanoate Injection IP (50 mg / mL)

Healthy Inc offers Nandrolone Decanoate Injection IP, a potent Anabolic Androgenic Steroid (AAS) designed for long-acting therapeutic effects. Containing Nandrolone Decanoate 50 mg, this formulation is a clinical priority for the management of Anemia associated with Chronic Renal Failure, Refractory Anemias, and the treatment of Postmenopausal Osteoporosis. It is also an essential adjunctive therapy for reversing negative nitrogen balance in Chronic Wasting Diseases and severe trauma. As a specialized Indian export partner, we supply this metabolic therapeutic to nephrology units, geriatric clinics, and oncology support centers in global pharmaceutical markets.

• Clinical Efficacy: Promotes protein synthesis and bone mineral density with a high anabolic-to-androgenic ratio. The decanoate ester ensures a slow release into the bloodstream, providing a sustained therapeutic effect for up to 3–4 weeks from a single dose.

• Manufacturing: Produced in associated WHO-GMP certified sterile facilities. The oil-based injection is formulated under strict aseptic conditions to ensure 100% sterility, high molecular purity, and consistent viscosity for Deep Intramuscular (IM) administration.

• Climate Stability: Validated for Zone IVb (Hot/Humid) conditions; the oil carrier and active ester are stabilized to prevent oxidation and degradation across Africa, LATAM, and SEA markets.

• Regulatory Support: Full technical documentation available, including CTD/eCTD Dossiers, to streamline the registration of specialized hormonal and anabolic therapies.

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

Available strengths and packaging? We supply Nandrolone Decanoate in the 50 mg / mL strength, as well as 25 mg/mL and 100 mg/mL. It is available in 1 mL ampoules, pre-filled syringes, or multi-dose vials. 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 product is Zone IVb stability-tested. We utilize neutral USP Type I glass and specialized moisture-resistant secondary packaging to ensure the chemical integrity of the steroid 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 Nandrolone Decanoate with other hormonal injectables (such as Testosterone or Hydrocortisone) and nutritional supplements 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 oversight for essential anabolic and metabolic care. 

Product Price :Get Latest Price

Product Details:

Each 3ml Contains Thiamine HCL I.P 100 Mg + Riboflavin Sodium Phosphate I.P. 5mg + Pyridoxine HCL I.P 100 Mg + Cyanocobalamin I.P 1000 Mcg + Nicotinamide I.P 100 Mg + D-Panthenol I.P. 50 Mg + Benzyl Alcohol I.P. 09% (As Preservative) Water For Injection IP Q.s.
NEURO-N-NURO Injection (Methylcobalamin, Pyridoxine & Nicotinamide)

Healthy Inc offers NEURO-N-NURO, a high-potency Neurotropic B-Vitamin Combination designed for intensive nerve repair and metabolic restoration. This synergistic formulation combines Methylcobalamin (the active form of B12) with Pyridoxine (B6) and Nicotinamide (B3). It is a clinical priority for treating Peripheral Neuropathy, Diabetic Retinopathy, Alcoholic Neuropathy, and severe vitamin deficiencies that manifest as neurological impairment. As a specialized Indian export partner, we supply this essential neuro-regenerative therapeutic to neurology clinics and general hospital networks in global pharmaceutical markets.

• Synergistic Nerve Repair: Methylcobalamin promotes the synthesis of the myelin sheath, while Pyridoxine and Nicotinamide support neurotransmitter synthesis and cellular energy production, accelerating the recovery of damaged peripheral nerves.

• Manufacturing: Produced in associated WHO-GMP certified sterile facilities. The formulation is engineered for high molecular stability and 100% sterility, suitable for Intramuscular (IM) or slow Intravenous (IV) administration.

• Climate Stability: Validated for Zone IVb (Hot/Humid) conditions; vitamins are highly sensitive to environmental factors, so NEURO-N-NURO is stabilized to ensure potency across Africa, LATAM, and SEA markets.

• Regulatory Support: Full technical documentation available, including CTD/eCTD Dossiers, to streamline the registration of neurotropic and nutritional injectables.

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

Available strengths and packaging? We supply NEURO-N-NURO in 2 mL and 5 mL ampoules/vials. Typical concentrations include Methylcobalamin 1000 mcg or 1500 mcg, paired with balanced doses of B6 and B3. Every batch undergoes rigorous HPLC-based assay testing and sterility validation.

Support for tropical export? Yes. Vitamin B-complex molecules are highly sensitive to light and heat. NEURO-N-NURO is Zone IVb stability-tested, and we utilize neutral USP Type I amber glass and light-shielding secondary packaging to prevent degradation 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 tender participations in your specific territory.

Small-volume or mixed orders? We specialize in mixed-container consolidation, allowing you to combine NEURO-N-NURO with other neurological or supportive care injectables (such as Thiamine, Folic Acid, or Gabapentin alternatives) 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 neuro-therapeutic care.

Approx. Rs 21.66 / PieceGet Latest Price

Product Details:

Pantoprazole Injection 40mg
PANTOPRAZOLE for Injection BP/USP (40 mg Lyophilized)

Healthy Inc offers Pantoprazole 40 mg, a high-precision Proton Pump Inhibitor (PPI) and a cornerstone in hospital-grade gastrointestinal care. Containing Pantoprazole Sodium 40 mg, this formulation is a clinical priority for the rapid suppression of gastric acid in patients for whom oral therapy is not feasible. It is a frontline therapeutic for Acute Gastroesophageal Reflux Disease (GERD), Zollinger-Ellison Syndrome, and the prophylaxis of Stress Ulcers in Intensive Care Units (ICUs). As a specialized Indian export partner, we supply this essential injectable to surgical units, emergency departments, and hospital networks in global pharmaceutical markets.

• Clinical Efficacy: Irreversibly binds to the H+/K+-ATPase enzyme system (the gastric acid pump) of the parietal cells, providing a potent and sustained 24-hour reduction in acid secretion, facilitating rapid mucosal healing and stabilization of pH.

• Manufacturing Excellence: Produced in associated WHO-GMP certified facilities specialized in Sterile Lyophilization. The freeze-drying process ensures maximum molecular stability, 100% sterility, and instantaneous, residue-free reconstitution for Intravenous (IV) administration.

• Climate Stability: Validated for Zone IVb (Hot/Humid) conditions; the lyophilized powder form is engineered to resist thermal degradation and maintain 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 hospital-grade gastrointestinal therapeutics.

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

Available strengths and packaging? We supply Pantoprazole in the 40 mg strength. The vial is often supplied in a "Combi-pack" containing a 10 mL sterile diluent (0.9% Sodium Chloride) for immediate clinical use. Every batch undergoes rigorous HPLC-based assay testing and sterility validation to meet international pharmacopoeia standards.

Support for tropical export? Yes. Our Pantoprazole is Zone IVb stability-tested. We utilize neutral USP Type I glass vials and moisture-resistant secondary packaging to ensure the product remains stable 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 healthcare tender participations in your specific territory.

Small-volume or mixed orders? We specialize in mixed-container consolidation, allowing you to combine Pantoprazole 40 mg with other gastrointestinal or critical care injectables (such as Ondansetron, Ranitidine, 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 essential acid-suppression therapies.

Approx. Rs 424.58 / PieceGet Latest Price

Product Details:

Cefoperazone 500mg & Sulbactam 500mg
SAFEZONE SB Injection (Ceftriaxone 500 mg + Sulbactam 500 mg)

Healthy Inc offers SAFEZONE SB 1g, a decisive-spectrum antibacterial combination designed to overcome bacterial resistance in clinical settings. This formulation contains a total of 1g of active ingredients, split between Ceftriaxone (500 mg) and Sulbactam (500 mg). It is a clinical priority for treating moderate to severe bacterial infections, particularly when $\beta$-lactamase-mediated resistance is suspected.

•  Synergistic Mechanism: Ceftriaxone provides potent bactericidal activity against a wide range of pathogens by inhibiting cell wall synthesis.  Sulbactam acts as a "shield," irreversibly inhibiting $\beta$-lactamase enzymes that would otherwise deactivate the antibiotic, thereby restoring its full clinical efficacy.

   

• Manufacturing Excellence: Produced in associated WHO-GMP certified sterile facilities. The sterile dry powder for injection is manufactured under strict aseptic conditions to ensure 100% sterility, high molecular purity, and rapid, residue-free reconstitution for Intravenous (IV) or Intramuscular (IM) use.

• Clinical Utility: Frequently utilized for pediatric infections, moderate community-acquired pneumonia, and specialized surgical prophylaxis where a 1g dose is clinically indicated.

• Climate Stability: Validated for Zone IVb (Hot/Humid) conditions; the dry powder format is engineered for high stability, ensuring consistent potency throughout international transit to Africa, LATAM, and SEA markets.

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

Available strengths and packaging?

We supply SAFEZONE SB in the 1g (500mg+500mg) and the 1.5g (1000mg+500mg) strengths. Each unit is presented in a USP Type I glass vial, typically accompanied by sterile Water for Injection. Every batch undergoes rigorous HPLC-based assay testing and sterility validation.

Support for tropical export?

Yes. SAFEZONE SB 1g is Zone IVb stability-tested. We utilize moisture-resistant secondary packaging and neutral glass vials to ensure the product remains stable and free from 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 institutional tender participations in your specific territory.

Small-volume or mixed orders?

We specialize in mixed-container consolidation, allowing you to combine SAFEZONE SB with other essential antibiotics (such as Amoxicillin-Clavulanate or Meropenem) in a single, cost-effective shipment.

Approx. Rs 8,130.00 / VialGet Latest Price

Product Details:

mycobacterium w 0.5×10⁹ bacilli + sodium chloride 0.9% w/v + thiomersal 0.01% w/v
SEPSIVAC Injection (Heat-Killed Mycobacterium w)

Healthy Inc offers SEPSIVAC, a pioneering immunomodulator containing heat-killed Mycobacterium w ($Mw$). Developed by Cadila Pharmaceuticals, 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, potentially 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.

• 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. 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 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 28.13 / BoxGet Latest Price

Product Details:

Sodium Chloride Injection IP 0.9%w/v
Sodium Chloride Injection IP (0.9% w/v) — Normal Saline

Healthy Inc offers Sodium Chloride Injection IP (0.9%), the fundamental isotonic crystalloid solution for clinical fluid resuscitation. Often referred to as Normal Saline, each 100 mL contains 0.9 g of Sodium Chloride, providing approximately 154 mEq/L of Sodium and 154 mEq/L of Chloride. It is a clinical priority for extracellular fluid replacement, treatment of metabolic alkalosis in the presence of fluid loss, and as a primary diluent for the infusion of compatible drug additives.

 

• Isotonic Precision: Engineered to match the osmotic pressure of human blood, making it the safest vehicle for the rapid restoration of circulating blood volume in cases of dehydration, shock, or hemorrhage.

•  Manufacturing Excellence: Produced in associated WHO-GMP certified facilities using advanced Blow-Fill-Seal (BFS) technology. This ensures a completely closed, sterile system that eliminates the risk of human-touch contamination and airborne particulates.

   

• Universal Compatibility: Acts as the standard vehicle for hundreds of IV medications. Our formulation is processed to be Pyrogen-free and Endotoxin-free, meeting the most stringent Indian Pharmacopoeia (IP) and international quality benchmarks.

• Climate Stability: Validated for Zone IVb (Hot/Humid) conditions; the specialized medical-grade polymer packaging is designed to resist environmental stress and maintain sterility across Africa, LATAM, and SEA markets.

Accepting B2B inquiries for bulk supply, institutional hospital tenders, and global export from our Mumbai logistics hub.

Available volumes and packaging? We supply Normal Saline (0.9%) in a wide range of sizes, including 10 mL and 20 mL ampoules for drug reconstitution, and 100 mL, 250 mL, 500 mL, and 1000 mL IV bags or BFS plastic bottles.

Support for tropical export? Yes. Our IV fluids are Zone IVb stability-tested. We utilize high-density, medical-grade plastic that prevents moisture loss and maintains chemical integrity even in high-temperature transit to tropical regions.

Registration assistance provided? We provide complete Regulatory Technical Files (CTD), Certificates of Analysis (COA), and manufacturing licenses to facilitate local health authority approvals and large-scale government healthcare tenders.

Mixed-container consolidation? Through our Mumbai hub, we can consolidate Sodium Chloride with other essential IV fluids (such as Dextrose 5%, Ringer's Lactate, or Mannitol) to provide a cost-effective, single-shipment solution for your hospital or distribution network.

Approx. Rs 14,062.50 / PieceGet Latest Price

Product Details:

Trastuzumab Injection 440 Mg With Wfi
TRASTUZUMAB for Injection (440 mg) with Sterile Water for Injection (WFI)

Healthy Inc offers Trastuzumab, a high-precision targeted biological therapy and a cornerstone in modern oncology. Containing 440 mg of Trastuzumab as a sterile, lyophilized powder, this formulation is a clinical priority for the treatment of HER2-positive Metastatic Breast Cancer and HER2-positive Gastric Cancer. As a specialized Indian export partner, we supply this advanced monoclonal antibody to oncology centers and tertiary care hospitals in global pharmaceutical markets.

• Targeted Mechanism: Trastuzumab is a recombinant DNA-derived humanized monoclonal antibody that selectively binds with high affinity to the extracellular domain of the Human Epidermal Growth Factor Receptor 2 (HER2). This inhibits the proliferation of tumor cells that overexpress HER2, providing a decisive therapeutic advantage over traditional non-targeted chemotherapy.

• Manufacturing Excellence: Produced in state-of-the-art biopharmaceutical WHO-GMP certified facilities. The Lyophilized (freeze-dried) format is engineered for maximum protein stability. Each pack is supplied with a dedicated vial of Sterile Water for Injection (WFI) containing a preservative (typically Bacteriostatic WFI) to ensure safe reconstitution and multi-dose stability.

• Therapeutic Superiority: Essential for both adjuvant treatment and metastatic management. Its use significantly improves disease-free survival rates in patients with HER2-overexpressing malignancies.

• Cold-Chain Integrity: As a complex protein-based therapeutic, Trastuzumab is highly temperature-sensitive. Our export protocols strictly maintain a $2^{\circ}\text{C}$ to $8^{\circ}\text{C}$ environment, utilizing digital data loggers and validated thermal shippers to guarantee molecular integrity from Mumbai to your clinical site.

Accepting B2B inquiries for institutional oncology supply, specialized tender participation, and global distribution from our Mumbai export hub.

B2B Technical Specifications

Cold-Chain Export Excellence

As a pharmacist-led firm, we prioritize the bio-stability of high-value monoclonal antibodies. We utilize Phase Change Material (PCM) technology in our packaging to ensure the temperature remains strictly within range during air freight, protecting your investment and patient safety.

Registration & Compliance Support

We provide comprehensive Regulatory Technical Files (CTD), including biosimilarity data and Batch Release Certificates, to facilitate local health authority approvals and participation in high-value government oncology tenders.

Oncology Consolidation

Through our Mumbai hub, we can consolidate Trastuzumab with other oncology essentials—such as Paclitaxel, Docetaxel, or Ondansetron—to provide a complete treatment regimen in a single, secure shipment.

Approx. Rs 50 / PieceGet Latest Price

Product Details:

AMOXICILLIN SODIUM Injection (500 mg)

Healthy Inc offers Amoxicillin Sodium Injection, a high-purity, broad-spectrum $\beta$-lactam antibiotic. Containing 500 mg of sterile Amoxicillin Sodium, this injectable is an essential clinical tool for the rapid treatment of severe bacterial infections where oral administration is ineffective or contraindicated. As a specialized Indian export partner, we supply this fundamental anti-infective to hospitals, clinics, and government health departments globally.

• Broad-Spectrum Bactericidal Action: Amoxicillin acts by inhibiting the final transpeccidation step of peptidoglycan synthesis in the bacterial cell wall. It is highly effective against a wide range of Gram-positive and Gram-negative pathogens, including Streptococcus spp., Listeria monocytogenes, and H. influenzae.

• Clinical Versatility: Indicated for severe Lower Respiratory Tract Infections (LRTI), acute Otitis Media, complicated Urinary Tract Infections (UTIs), and Septicemia. It is also a critical component in the treatment of bacterial Meningitis due to its ability to reach therapeutic concentrations in the CSF when meninges are inflamed.

• Manufacturing Excellence: Produced in associated WHO-GMP certified sterile dry-powder facilities. The formulation is micronized to ensure immediate, residue-free reconstitution, providing a clear solution for safe 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 and prevent degradation during international transit to Africa, LATAM, and SEA markets.

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

B2B Trade Specifications

Logistics & Export Optimization

As a pharmacist-led firm, we understand that sterile powders like Amoxicillin Sodium are highly sensitive to moisture ingress. We utilize specialized moisture-barrier secondary packaging and impact-resistant cartons to ensure the product reaches your clinical facility in peak condition, while optimizing pallet space to reduce per-unit freight costs 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 NGO-led tenders.

Approx. Rs 50 / PieceGet Latest Price

Product Details:

CLOXACILLIN Injection (1 gm)

Healthy Inc offers Cloxacillin Sodium Injection in the high-potency 1 gm strength. This formulation is a sterile, dry-powder penicillinase-resistant penicillin, specifically engineered to treat severe systemic infections caused by $\beta$-lactamase-producing Staphylococci. As a specialized Indian export partner, we supply this clinical essential to surgical wards, orthopedic units, and intensive care departments globally from our Mumbai export hub.

• Targeted Bactericidal Action: Cloxacillin is designed with a bulky side chain that sterically hinders the action of the bacterial enzyme penicillinase. This allows the molecule to bind to penicillin-binding proteins (PBPs) and inhibit cell wall synthesis in strains that are otherwise resistant to standard penicillins like Ampicillin.

• Clinical Criticality for Severe Infections: The 1 gm strength is a priority for managing life-threatening conditions including Osteomyelitis (bone infections), Septic Arthritis, Endocarditis, and severe Septicemia caused by Methicillin-Susceptible Staphylococcus aureus (MSSA).

• Surgical & Trauma Utility: It is widely utilized in the prevention and treatment of post-operative surgical site infections, particularly in orthopedic and cardiothoracic surgeries where staphylococcal contamination is a high risk.

• Manufacturing Excellence: Produced in associated WHO-GMP certified sterile facilities. The powder is micronized to ensure instant, residue-free reconstitution, providing a clear solution for Intravenous (IV) or Intramuscular (IM) administration.

Accepting B2B inquiries for high-volume supply, institutional healthcare tenders, and contract manufacturing.

B2B Technical Specifications

Logistics & Stability Management

As a pharmacist-led firm, we understand that Cloxacillin is highly hygroscopic. Exposure to moisture during transit can lead to degradation, resulting in a loss of potency and distinct discoloration (browning). We utilize specialized moisture-barrier secondary packaging and high-integrity vacuum-sealed vials to ensure the product maintains 100% molecular stability during international transit to Africa, LATAM, and SEA markets.

Approx. Rs 11.31 / VialGet Latest Price

Product Details:

Sodium Bicarbonate Injection
SODIUM BICARBONATE Injection (7.5% w/v / 8.4% w/v)

Healthy Inc offers Sodium Bicarbonate Injection, a critical systemic alkalizing agent and electrolyte replenisher. As a pharmacist-led firm, we supply this essential "crash-cart" medication primarily for the rapid reversal of metabolic acidosis in emergency and critical care settings. Produced in associated WHO-GMP certified large-volume parenteral (LVP) facilities, our formulation is managed with high precision from our Mumbai export hub.

• Acid-Base Neutralization Mechanism: Sodium Bicarbonate dissociates in the plasma to provide bicarbonate ions ($HCO_3^-$). These ions act as a direct buffer against excess hydrogen ion ($H^+$) concentrations, raising the blood pH and reversing states of metabolic acidosis.

• Clinical Criticality: Indicated for the treatment of Metabolic Acidosis occurring in severe renal disease, uncontrolled diabetes (DKA), and circulatory insufficiency due to shock or severe dehydration. It is a frontline therapeutic during Cardiac Arrest to manage the buildup of lactic acid and is used as an adjunct in certain drug toxicologies (e.g., Tricyclic Antidepressant or Aspirin overdose) to promote urinary alkalinization.

• Electrolyte Management: It is also utilized in the emergency management of Hyperkalemia, as the shift in pH facilitates the movement of potassium from the extracellular space into the cells.

• Manufacturing Excellence: Formulated as a sterile, non-pyrogenic solution. Due to the risk of carbon dioxide ($CO_2$) buildup during storage, our production involves strict head-space control. We provide this in USP Type I glass vials or specialized infusion bottles to ensure the chemical integrity of the alkalizing solution.

B2B Technical Specifications Logistics & Export Optimization

As a pharmacist, you understand that Sodium Bicarbonate is chemically incompatible with many common IV drugs (such as Calcium salts, Catecholamines, or certain Antibiotics), as it can cause immediate precipitation. We provide clear compatibility labeling and technical data sheets to assist clinical staff. Our logistics team optimizes shipments to Africa, LATAM, and SEA, ensuring that the primary containers are protected from thermal shocks that could lead to glass breakage or $CO_2$ pressure issues in Zone IVb climates.

Approx. Rs 20.63 / BoxGet Latest Price

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Alfacalcidol 0.25 Mcg
ALFACALCIDOL Softgel Capsules (0.25 mcg / 0.5 mcg / 1 mcg)

Healthy Inc offers Alfacalcidol Softgel Capsules, a potent Vitamin D3 analogue ($1\alpha\text{-hydroxyvitamin } D_3$). As a pharmacist-led export firm, we recognize this as a critical therapeutic for patients with impaired renal function who cannot activate standard Vitamin D. Produced in associated WHO-GMP certified facilities, our Alfacalcidol is engineered for rapid absorption and consistent hormonal activity, managed from our Mumbai export hub.

• Hepatic Activation Mechanism: Unlike Cholecalciferol (standard $D_3$), which requires both hepatic and renal hydroxylation to become active, Alfacalcidol is a prodrug that only requires 25-hydroxylation in the liver. It bypasses the kidneys, making it the clinical gold standard for patients with chronic kidney disease (CKD) or renal failure.

• Calcium Homeostasis: Once converted to Calcitriol (the active metabolite), it increases the intestinal absorption of calcium and phosphate, regulates bone mineralization, and suppresses excessive parathyroid hormone (PTH) secretion.

• Clinical Indications: Primarily indicated for Renal Osteodystrophy, Hypoparathyroidism, and Vitamin D-resistant rickets. It is also highly effective in managing post-menopausal and corticosteroid-induced Osteoporosis to reduce fracture risk.

• Softgel Superiority: Our Alfacalcidol is formulated in a Soft Gelatin Capsule with a lipid-based vehicle. This ensures maximum stability of the sensitive molecule and superior bioavailability, as Vitamin D analogues are fat-soluble and require a lipid matrix for optimal absorption in the GI tract.

B2B Technical Specifications Logistics & Export Optimization

As a pharmacist, you know that Alfacalcidol is highly oxygen and light-sensitive. Degradation of the sterol structure leads to a complete loss of therapeutic potency. We utilize Alu-Alu blister packaging to provide a superior moisture and light barrier. Our logistics team optimizes shipments to Africa, LATAM, and SEA, ensuring the product is stored in "Cool & Dry" conditions during transit from Mumbai to prevent the softgels from clumping or leaking in Zone IVb climates.

Approx. Rs 29.91 / BoxGet Latest Price

Product Details:

Amoxycillin 250mg And Cloxacillin 250mg Capsules
AMOXYCILLIN & CLOXACILLIN Capsules (250 mg + 250 mg)

Healthy Inc offers the Amoxycillin & Cloxacillin combination, a synergistic dual-penicillin therapeutic. This formulation is specifically designed to broaden the antibacterial spectrum and overcome the limitations of single-agent therapy against penicillinase-producing organisms. As a specialized Indian export partner, we supply this high-demand antibiotic combination to primary care clinics and surgical centers globally from our Mumbai export hub.

• Synergistic Mechanism of Action:

  • Amoxycillin: A moderate-spectrum penicillin that provides robust coverage against a wide range of Gram-positive and Gram-negative bacteria by inhibiting cell wall synthesis.

  • Cloxacillin: An antistaphylococcal (penicillinase-resistant) penicillin. It binds to and inhibits the beta-lactamase enzymes produced by Staphylococcus aureus, which would otherwise deactivate the Amoxycillin.

• Clinical Criticality: This "Twin-Penicillin" combo is a frontline choice for mixed bacterial infections, post-operative wound care, and specialized infections like osteomyelitis, septicemia, and severe respiratory tract infections where resistant Staphylococci are suspected.

• Pharmacokinetic Profile: Both active ingredients are acid-stable and well-absorbed from the GI tract. The combination ensures that therapeutic concentrations are achieved in various body fluids and tissues, providing a comprehensive "shield" against complex infections.

• Manufacturing Excellence: Produced in associated WHO-GMP certified facilities. Our capsules are manufactured using high-grade Amoxycillin Trihydrate and Cloxacillin Sodium, ensuring molecular stability and precise 1:1 dosing ratios.

B2B Technical Specifications Logistics & Export Optimization

As a pharmacist, you are aware that both ingredients, especially Cloxacillin Sodium, are highly hygroscopic. Exposure to humidity can lead to degradation of the beta-lactam ring and clumping of the capsule contents. We utilize Alu-Alu blister packaging as a mandatory standard for this product to provide a total barrier against moisture. Our logistics team optimizes shipments to Africa, LATAM, and SEA, ensuring stability in Zone IVb (Hot/Humid) climates through moisture-controlled transit from Mumbai.

Approx. Rs 32.82 / StripGet Latest Price

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Amoxycillin Capsules IP 500mg

AMOXYCILLIN Capsules IP 500 mg

Healthy Inc offers Amoxycillin Capsules IP 500 mg, a high-velocity moderate-spectrum beta-lactam antibiotic manufactured to the stringent quality standards of the Indian Pharmacopoeia (IP). As a pharmacist-led export partner, we recognize that the 500 mg IP-grade capsule is the global clinical standard for adult dosing in acute bacterial infections. Managed through our Mumbai export hub, this formulation is optimized for superior acid stability and maximum systemic bioavailability.

• Bactericidal Mechanism: Amoxycillin IP works by inhibiting bacterial cell wall synthesis. It competitively inhibits the transpeptidase enzymes (Penicillin-Binding Proteins or PBPs) responsible for cross-linking the peptidoglycan layers of the bacterial cell wall. This disruption leads to osmotic instability and subsequent cell lysis.

• Target Pathogen Spectrum: It provides robust coverage against a variety of Gram-positive and select Gram-negative organisms, including Streptococcus spp., Haemophilus influenzae, and Helicobacter pylori.

• Clinical Criticality: The 500 mg dosage is a frontline therapeutic for Community-Acquired Pneumonia (CAP), acute exacerbations of chronic bronchitis, dental abscesses, and severe urinary tract infections. It is also a fundamental component of "triple therapy" for gastric ulcer management.

• IP Standard Compliance: Every batch is tested against the rigorous monographs of the Indian Pharmacopoeia, ensuring strict adherence to parameters for assay, dissolution, and moisture content, providing a reliable and cost-effective alternative to innovator brands.

B2B Technical Specifications Logistics & Export Optimization

As a pharmacist, you are aware that Amoxycillin Trihydrate is highly sensitive to environmental humidity. Moisture ingress can trigger the hydrolysis of the beta-lactam ring, compromising efficacy. We utilize Alu-Alu blister packaging as a gold standard for all our exports to Africa, LATAM, and SEA. This provides a 100% barrier against moisture and oxygen, ensuring the stability of the IP-grade powder in Zone IVb (Hot/Humid) climates throughout the transit from Mumbai.

Approx. Rs 100 / BoxGet Latest Price

Product Details:

DEXRABEPRAZOLE SODIUM & DOMPERIDONE Capsules

Healthy Inc offers the Dexrabeprazole Sodium and Domperidone combination, a high-efficiency therapeutic for the management of chronic acid-peptic disorders and associated dyspepsia. As a pharmacist-led firm, we recognize this combination as a "refined" GI solution, utilizing the R-enantiomer of Rabeprazole to provide potent acid suppression with a superior safety profile. Managed through our Mumbai export hub, this formulation is engineered for rapid symptomatic relief and improved patient compliance.

• Enantiomeric Synergy:

  • Dexrabeprazole Sodium: The active (R)-enantiomer of Rabeprazole. It is a Proton Pump Inhibitor (PPI) that exhibits higher potency than racemic Rabeprazole, allowing for a lower effective dose (typically 10 mg vs. 20 mg). It provides faster onset of acid suppression and has a more predictable metabolic profile.

  • Domperidone: A peripheral Dopamine ($D_2$) receptor antagonist. It serves as a prokinetic agent by increasing esophageal sphincter tone and enhancing gastric motility. This helps prevent the physical reflux of stomach acid and alleviates symptoms of bloating and fullness.

• Clinical Criticality: Indicated for the treatment of Gastroesophageal Reflux Disease (GERD), functional dyspepsia, and chronic gastritis. It is particularly effective for patients who experience "nocturnal acid breakthrough" or those with delayed gastric emptying.

• The Dex-Advantage: Because Dexrabeprazole is less dependent on the CYP2C19 liver enzyme for metabolism, it offers a more consistent therapeutic effect across different patient genotypes (Fast vs. Slow metabolizers) compared to older PPIs like Omeprazole.

• Manufacturing Excellence: Produced in associated WHO-GMP certified facilities. Our capsules utilize dual-pelletization technology, featuring enteric-coated Dexrabeprazole to prevent premature degradation in stomach acid and sustained-release Domperidone for round-the-clock prokinetic support.

B2B Technical Specifications Logistics & Export Optimization

As a pharmacist, you are aware that Dexrabeprazole Sodium is highly hygroscopic and acid-labile. Any exposure to moisture during transit can compromise the enteric coating of the pellets, leading to drug failure. We utilize Alu-Alu blister packaging as an absolute requirement for this product. Our logistics team optimizes shipments to Africa, LATAM, and SEA, ensuring the stability of the enantiomeric salt in Zone IVb (Hot/Humid) climates through moisture-controlled transit from Mumbai.

Approx. Rs 100 / StripGet Latest Price

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DOXEPIN HYDROCHLORIDE Capsules (10 mg / 25 mg / 50 mg / 75 mg)

Healthy Inc offers Doxepin Hydrochloride Capsules, a versatile Tricyclic Antidepressant (TCA) with potent antihistaminic properties. As a pharmacist-led firm, we recognize Doxepin as a multi-functional therapeutic utilized across psychiatry, neurology, and dermatology. Managed through our Mumbai export hub, our formulation is produced in associated WHO-GMP certified facilities, ensuring rigorous control over purity and dissolution profiles.

• Multi-Targeted Mechanism of Action: Doxepin exerts its effects through several pathways:

  • Neurotransmitter Reuptake Inhibition: It inhibits the reuptake of Norepinephrine and, to a lesser extent, Serotonin at the presynaptic terminals, which helps alleviate depressive symptoms.

  • Potent Antihistaminic Activity: Doxepin has a very high affinity for $H_1$ and $H_2$ receptors, making it significantly more potent than many standard antihistamines. This explains its efficacy in treating chronic pruritus and insomnia.

  • Anticholinergic & Alpha-Adrenergic Blockade: These secondary actions contribute to its sedative profile and clinical utility in specific pain syndromes.

• Clinical Versatility:

  • Psychiatry: Treatment of depression and anxiety associated with psychoneurosis.

  • Neurology & Pain: Management of chronic tension-type headaches and neuropathic pain.

  • Sleep Medicine: Low-dose therapy for sleep maintenance insomnia.

  • Dermatology: Management of severe chronic urticaria and intractable pruritus.

• Pharmacokinetic Profile: Doxepin is well-absorbed from the GI tract and undergoes significant first-pass metabolism in the liver to its active metabolite, Nordoxepin (Desmethyldoxepin). This metabolite extends the therapeutic half-life, supporting sustained clinical effects.

• Manufacturing Excellence: We ensure the stability of the Hydrochloride salt and the uniformity of the micronized API within the capsule to guarantee consistent release, which is critical for titration and minimizing dose-dependent side effects.

B2B Technical Specifications Logistics & Export Optimization

As a pharmacist, you are aware that Doxepin Hydrochloride can be sensitive to photo-degradation. We utilize opaque capsule shells and light-resistant secondary packaging to ensure molecular integrity. For exports to Africa, LATAM, and SEA, our logistics team maintains strict inventory controls and "Dry-Cargo" protocols from Mumbai, ensuring the stability of the TCA profile in Zone IVb climates.

Approx. Rs 330.15 / BoxGet Latest Price

Product Details:

Esomeprazole 40mg & Levosulpiride 75mg
ESOMEPRAZOLE & LEVOSULPIRIDE Capsules

Healthy Inc offers the Esomeprazole (Delayed Release) and Levosulpiride (Sustained Release) combination, a premium therapeutic for the management of complex acid-peptic disorders and functional dyspepsia. As a pharmacist-led firm, we recognize this as a "gold-standard" pairing for patients who do not respond to PPI monotherapy. Managed from our Mumbai export hub, this formulation is produced in associated WHO-GMP facilities using advanced multi-particulate pellet technology.

• Pharmacological Synergy:

  • Esomeprazole (40 mg): The S-isomer of Omeprazole. It is a highly potent Proton Pump Inhibitor (PPI) that provides more effective and sustained acid suppression than its racemic predecessor. It works by irreversibly inhibiting the $H^+/K^+$-ATPase enzyme system in the gastric parietal cells.

  • Levosulpiride (75 mg SR): The purified levo-isomer of Sulpiride. It acts as a selective Dopamine ($D_2$) receptor antagonist with prokinetic properties. It enhances gastrointestinal motility and increases the tone of the lower esophageal sphincter (LES), preventing the retrograde flow of gastric contents.

• Clinical Indications:

  • Gastroesophageal Reflux Disease (GERD): Specifically for refractory cases with prominent regurgitation.

  • Functional Dyspepsia: Relief from bloating, early satiety, and postprandial fullness.

  • Irritable Bowel Syndrome (IBS): Where dyspeptic symptoms are a significant component.

• The "Levo" Advantage: Unlike older prokinetics, Levosulpiride exhibits a significantly lower incidence of extrapyramidal side effects and offers additional anti-emetic and mood-stabilizing benefits at low doses, improving overall patient quality of life.

• Manufacturing Excellence: Our capsules utilize dual-pelletization technology. The Esomeprazole pellets are enteric-coated to prevent acid-catalyzed degradation, while the Levosulpiride pellets are engineered for a sustained-release (SR) profile to maintain prokinetic efficacy for 24 hours.

B2B Technical Specifications Logistics & Export Optimization

As a pharmacist, you are aware that Esomeprazole Sodium is highly hygroscopic and acid-labile. If the enteric coating of the pellets is compromised by moisture, the medication will fail in the stomach. We utilize Alu-Alu blister packaging exclusively for this product to provide a 100% moisture barrier. Our logistics team optimizes shipments to Africa, LATAM, and SEA, ensuring the stability of the pellet matrix in Zone IVb (Hot/Humid) climates throughout the transit from Mumbai.

Approx. Rs 1,850.00 / BoxGet Latest Price

Product Details:

Esomeprazole 40Mg + Domperidone 30Mg
ESOMEPRAZOLE & DOMPERIDONE Capsules (40 mg + 30 mg SR)

Healthy Inc offers the Esomeprazole and Domperidone (Sustained Release) fixed-dose combination, a specialized therapeutic for the management of refractory gastroesophageal disorders. As a pharmacist-led firm, we recognize this pairing as the preferred choice for patients who experience acid reflux complicated by gastric dysmotility. Managed through our Mumbai export hub, our formulation utilizes advanced multi-particulate pellet technology to ensure dual-phase drug delivery.

• Pharmacological Synergy:

  • Esomeprazole (40 mg): The S-enantiomer of Omeprazole. It provides more potent and longer-lasting acid suppression by irreversibly inhibiting the $H^+/K^+$-ATPase (proton pump) in the gastric parietal cells.

  • Domperidone (30 mg SR): A peripheral Dopamine ($D_2$) receptor antagonist. It acts as a prokinetic agent, increasing lower esophageal sphincter (LES) tone and accelerating gastric emptying.

• Clinical Criticality: Indicated for the treatment of Gastroesophageal Reflux Disease (GERD) and Functional Dyspepsia. It is particularly effective for patients presenting with "acid-regurgitation" and symptoms of bloating or "heaviness" after meals, which often indicate delayed gastric transit.

• The S-Isomer Advantage: Esomeprazole exhibits higher systemic exposure and more predictable pharmacokinetics compared to racemic PPIs. Because it is less dependent on the CYP2C19 liver enzyme, it offers a consistent therapeutic response across varied patient genotypes.

• Manufacturing Excellence: Produced in associated WHO-GMP certified facilities. Our capsules utilize dual-pelletization: Esomeprazole pellets are enteric-coated (EC) to bypass stomach acid, while Domperidone is formulated as sustained-release (SR) pellets to maintain pro-motility action throughout the day.

B2B Technical Specifications Logistics & Export Optimization

As a pharmacist, you are aware that Esomeprazole is highly hygroscopic and acid-labile. Moisture ingress can cause the enteric coating of the pellets to fail, leading to drug degradation in the stomach. We utilize Alu-Alu blister packaging as a mandatory standard for all our exports to Africa, LATAM, and SEA. This provides a 100% barrier against humidity, ensuring the stability of the 40+30 mg matrix in Zone IVb (Hot/Humid) climates throughout the transit from Mumbai.

Approx. Rs 154.65 / BoxGet Latest Price

Product Details:

omeprazole 20 mg + domperidone 10 mg
OMEPRAZOLE & DOMPERIDONE Capsules (20 mg + 10 mg / 30 mg SR)

Healthy Inc offers the Omeprazole and Domperidone combination, a frontline therapeutic for dyspeptic disorders. As a pharmacist-led firm, we recognize this as a "standard-of-care" for patients presenting with acid reflux complicated by gastric stasis. Managed through our Mumbai export hub, our formulation is produced in associated WHO-GMP facilities using precision dual-pellet technology.

Pharmacological Synergy

This combination addresses the two primary physiological drivers of gastroesophageal reflux:

• Omeprazole (20 mg): A substituted benzimidazole that acts as a Proton Pump Inhibitor (PPI). It irreversibly binds to the $H^+/K^+$-ATPase enzyme system at the secretory surface of the gastric parietal cell, suppressing both basal and stimulated acid secretion.

• Domperidone (10 mg / 30 mg SR): A peripheral Dopamine ($D_2$) receptor antagonist. It acts as a prokinetic agent by increasing esophageal peristalsis and enhancing the tone of the lower esophageal sphincter (LES). It simultaneously accelerates gastric emptying, ensuring that acid and food do not "pool" in the stomach.

Clinical Indications

• Gastroesophageal Reflux Disease (GERD): Relief from heartburn and acid regurgitation when symptoms are not controlled by PPIs alone.

• Dyspeptic Symptom Complex: Management of epigastric pain, bloating, and early satiety.

• Nausea & Vomiting: Prevention of acid-induced nausea associated with chronic gastritis.

B2B Technical Specifications Logistics & Export Optimization

As a pharmacist, you are aware that Omeprazole is exceptionally acid-labile. If the enteric coating on the pellets is compromised by moisture or heat during transit, the drug will degrade in the stomach's acid before reaching the site of absorption in the small intestine.

Approx. Rs 100 / BoxGet Latest Price

Product Details:

OMEPRAZOLE Delayed-Release Capsules (40 mg)

Healthy Inc offers Omeprazole 40 mg, the high-strength presentation of the definitive Proton Pump Inhibitor (PPI). As a pharmacist-led organization, we recognize that while the 20 mg dose is the standard for general reflux, the 40 mg concentration is the clinical requirement for intensive acid suppression in severe erosive conditions and hypersecretory states. Managed through our Mumbai export hub, our formulation is produced in associated WHO-GMP certified facilities using advanced micropelletization technology.

Pharmacological Profile

• Mechanism of Action (The "Proton Pump" Blockade): Omeprazole is a substituted benzimidazole prodrug. Once activated in the acidic environment of the gastric parietal cell's canaliculi, it irreversibly binds to the $H^+/K^+$-ATPase enzyme system. This action shuts down the "proton pump," the final pathway for hydrochloric acid secretion into the stomach lumen.

• The 40 mg Clinical Advantage: This higher dosage is specifically utilized when standard therapy is insufficient. It provides a more profound and sustained rise in intragastric pH, which is critical for:

  • Erosive Esophagitis: Healing severe (Grade C or D) mucosal damage.

  • Zollinger-Ellison Syndrome: Managing pathological gastric acid hypersecretion.

  • NSAID-Associated Ulcers: Preventing and healing ulcers in patients requiring chronic NSAID therapy.

  • Refractory GERD: Managing patients who do not achieve symptomatic relief with 20 mg daily.

• Enteric Protection Technology: Omeprazole is highly acid-labile. Our 40 mg capsules contain enteric-coated (EC) micropellets designed to remain stable in gastric acid (pH 1.2) and release the active drug only upon reaching the alkaline environment of the duodenum (pH >6.0).

B2B Technical Specifications Logistics & Export Optimization

As a pharmacist, you understand that Omeprazole is highly hygroscopic. High-strength 40 mg capsules are particularly sensitive; any moisture ingress can lead to pellet degradation, resulting in a color change (browning) and a drastic reduction in potency.