Veterinary Injection

Approx. Rs 6.76 / BoxGet Latest Price

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DICYCLOMINE HYDROCHLORIDE Injection (10 mg / mL)

Healthy Inc offers Dicyclomine Hydrochloride Injection, a specialized antispasmodic and anticholinergic agent. Containing 10 mg of sterile Dicyclomine HCl per mL, this injectable formulation is the clinical choice for the rapid relief of acute smooth muscle spasms within the gastrointestinal tract. As a pharmacist-led export firm, we supply this essential therapeutic to gastroenterology clinics and emergency departments globally from our Mumbai export hub.

• Dual-Action Spasmolysis: Dicyclomine provides a unique two-pronged approach. It acts as a competitive antagonist at muscarinic acetylcholine receptors and exerts a direct musculotropic effect on the smooth muscle of the GI tract. This combined action effectively reduces hypermotility and cramps with fewer side effects than traditional atropine-based treatments.

• Rapid Clinical Intervention: In acute settings where oral administration is impossible due to severe pain or vomiting, the 10 mg/mL injection provides near-instantaneous bioavailability, significantly reducing patient distress from intestinal, biliary, or renal colic.

• Indication Focus: Primarily indicated for functional bowel disorders and Irritable Bowel Syndrome (IBS) characterized by acute smooth muscle spasm.

• Manufacturing Excellence: Produced in associated WHO-GMP certified sterile facilities. The solution is formulated with precise pH stabilization to ensure patient comfort and 100% molecular bioavailability for Intramuscular (IM) administration.

B2B Technical Specifications Logistics & Export Optimization

As a pharmacist-led firm, we understand the critical nature of maintaining the physical integrity of glass ampoules during long-haul transit. We utilize custom-fit secondary packaging with internal shock-absorbing dividers to prevent breakage. Our logistics protocols for Africa, LATAM, and SEA markets include reinforced outer cartons specifically designed to withstand the high-humidity conditions of Zone IVb.

Registration & Compliance Support

We provide complete Regulatory Technical Files (CTD) and batch-specific Certificates of Analysis (COA). Our documentation is meticulously structured to facilitate rapid health authority approvals, ensuring that this essential antispasmodic meets the safety and purity requirements of both private hospital networks and government procurement agencies.

Approx. Rs 3.75 / StripGet Latest Price

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Pheniramine Maleate Injection IP 22.75 Mg
Pheniramine Maleate Injection IP (22.75 mg / mL)

Healthy Inc offers Pheniramine Maleate Injection IP, a highly effective First-Generation Antihistamine (H₁ receptor antagonist). Containing 22.75 mg per mL, this formulation is a clinical priority for the rapid management of acute allergic conditions, including anaphylactic shock, angioedema, urticaria, and allergic reactions to drugs or blood transfusions. As a specialized Indian export partner, we supply this essential emergency-care therapeutic to trauma centers, emergency departments, and general practitioners across global pharmaceutical markets.

• Clinical Precision: Effectively blocks H₁ receptors to alleviate symptoms like itching, swelling, and respiratory distress. Its rapid onset when administered via Intravenous (IV) or Intramuscular (IM) routes makes it an indispensable component of emergency "crash carts."

• Manufacturing Excellence: Produced in associated WHO-GMP certified sterile facilities. The solution is formulated under strict aseptic conditions to ensure 100% sterility, high molecular purity, and precise pH balance for safe systemic administration.

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

• Regulatory Support: Full technical documentation available, including CTD/eCTD Dossiers, to streamline the registration of essential emergency and allergy therapeutics.

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

Available strengths and packaging? We supply Pheniramine Maleate in the standard 22.75 mg / mL concentration, typically available in 2 mL ampoules or 10 mL multi-dose vials. Every batch undergoes rigorous HPLC-based assay testing and sterility validation to meet Indian Pharmacopoeia (IP) standards.

Support for tropical export? Yes. Our formulation is Zone IVb stability-tested. We utilize neutral USP Type I glass ampoules and moisture-resistant secondary packaging to ensure the product remains stable during international transit to high-temperature regions.

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

Small-volume or mixed orders? We specialize in mixed-container consolidation, allowing you to combine Pheniramine Maleate with other emergency or critical care injectables (such as Dexamethasone, Adrenaline, or Hydrocortisone) 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 allergy care.

Approx. Rs 15.94 / VialGet Latest Price

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Lignocaine Injection IP 2% W/v
Lignocaine Hydrochloride Injection IP (2% w/v)

Healthy Inc offers Lignocaine Hydrochloride 2%, a cornerstone Local Anesthetic of the amide group. Lignocaine (Lidocaine) is a clinical priority for inducing rapid-onset, intermediate-duration anesthesia by stabilizing neuronal membranes and preventing the conduction of nerve impulses. It is an essential agent for Infiltration Anesthesia, Minor Surgical Procedures, and Dental Blockade. In specialized emergency settings, it is also utilized for the acute management of Ventricular Arrhythmias. As a specialized Indian export partner, we supply this fundamental therapeutic to surgical centers, emergency departments, and dental clinics in global pharmaceutical markets.

• Rapid Onset: Known for its fast-acting properties, providing effective sensory blockade within minutes of administration.

• Manufacturing: Produced in associated WHO-GMP certified sterile facilities, ensuring 100% sterility, high molecular purity, and a precise 20 mg/ml concentration in strict compliance with Indian Pharmacopoeia (IP) standards.

• Climate Stability: Validated for Zone IVb (Hot/Humid) conditions, ensuring the chemical integrity and anesthetic potency of the molecule across Africa, LATAM, and SEA markets.

• Regulatory Support: Full technical documentation available, including CTD/eCTD Dossiers, to streamline the registration of essential 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 Lignocaine Hydrochloride 2% in 30 ml and 50 ml multi-dose vials, as well as 2 ml and 5 ml ampoules. Every batch undergoes rigorous HPLC-based assay testing, sterility validation, and pH stability checks to meet international pharmacopoeia standards.

Support for tropical export? Yes. Our formulation is Zone IVb stability-tested. We utilize neutral USP Type I glass and specialized export-grade secondary packaging to prevent molecular degradation during international transit to high-temperature regions.

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

Small-volume or mixed orders? We specialize in mixed-container consolidation, allowing you to combine Lignocaine with other surgical essentials (such as Bupivacaine, Adrenaline, or Ketorolac) in a single, cost-effective shipment.

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

Approx. Rs 24.34 / PieceGet Latest Price

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Cefotaxime Sodium 500mg
OMNATAX 500 mg Injection (Cefotaxime for Injection BP/USP 500 mg)

Healthy Inc offers OMNATAX 500, a versatile Third-Generation Cephalosporin Antibiotic optimized for pediatric, geriatric, and specialized adult dosing. Containing Cefotaxime Sodium 500 mg, OMNATAX is a clinical priority for treating moderate-to-severe infections including Bacterial Meningitis, Septicemia, Pneumonia, and Bone/Joint Infections. Due to its superior ability to penetrate the blood-brain barrier and its high stability against many beta-lactamases, it remains a frontline choice for hospital-acquired infections. As a specialized Indian export partner, we supply this essential anti-infective to pediatric wards, surgical units, and general hospitals in global pharmaceutical markets.

• Broad-Spectrum Control: Provides potent activity against Gram-negative pathogens (E. coli, Haemophilus influenzae, Klebsiella) and Gram-positive organisms (Streptococci), making it ideal for empirical therapy in vulnerable patient populations.

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

• Climate Stability: Validated for Zone IVb (Hot/Humid) conditions; the sterile powder form is engineered to maintain potency and stability 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 antibiotics.

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

Available strengths and packaging? We supply OMNATAX in the 500 mg strength, as well as 250 mg (Pediatric) and 1 g (Adult) presentations. The 500 mg vial is typically supplied with a sterile diluent (Sterile Water for Injection) to ensure precise reconstitution for immediate clinical use.

Support for tropical export? Yes. OMNATAX 500 is Zone IVb stability-tested. We utilize neutral USP Type I glass vials and moisture-resistant secondary packaging to ensure product integrity during international transit to high-temperature and high-humidity regions.

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

Small-volume or mixed orders? We specialize in mixed-container consolidation, allowing you to combine OMNATAX 500 with other critical care antibiotics (such as Ceftriaxone, Amikacin, or Metronidazole) in a single, cost-effective shipment.

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

Approx. Rs 50 / PieceGet Latest Price

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CLOXACILLIN Injection (500 mg)

Healthy Inc offers Cloxacillin Sodium Injection, a high-precision, penicillinase-resistant penicillin. Containing 500 mg of sterile Cloxacillin Sodium, this formulation is specifically engineered to target and neutralize $\beta$-lactamase-producing Staphylococci. As a specialized Indian export partner, we supply this essential antibiotic to surgical units and orthopedic clinics globally to combat resistant skin and soft tissue infections.

• Targeted Anti-Staphylococcal Action: Cloxacillin is chemically designed to resist degradation by the enzyme penicillinase (a type of $\beta$-lactamase). It remains the clinical gold standard for treating infections caused by penicillin-resistant Staphylococcus aureus (MSSA), ensuring bactericidal efficacy where standard penicillins fail.

• Clinical Versatility: Indicated for severe Skin and Soft Tissue Infections (cellulitis, abscesses), Osteomyelitis (bone infections), Septic Arthritis, and Endocarditis. It is also a critical component in post-operative wound management to prevent surgical site infections.

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

• Climate-Adaptive Stability: Validated for Zone IVb (Hot/Humid) conditions; vacuum-sealed in USP Type I glass vials with high-integrity bungs to maintain 100% molecular potency and prevent "caking" 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 Technical Specifications

Logistics & Export Optimization

As a pharmacist-led firm, we understand that Cloxacillin is highly hygroscopic. Moisture ingress can lead to rapid degradation and discoloration. 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 22.40 / BoxGet Latest Price

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Sodium Chloride 0.9% W/v

SODIUM CHLORIDE Intravenous Infusion (0.9% w/v)

Healthy Inc offers Sodium Chloride IV Infusion, commonly known as Normal Saline. As a pharmacist and CEO of a manufacturing and trading firm, you recognize this as the most fundamental fluid in clinical medicine. It serves as the primary vehicle for drug delivery and the first-line treatment for extracellular fluid replacement. Produced in WHO-GMP certified sterile facilities using Advanced Aseptic BFS (Blow-Fill-Seal) technology, these infusions are a high-volume cornerstone of our Mumbai-based export operations.

Product Usage & Clinical Applications

• Therapeutic Goal: To restore fluid and electrolyte balance and provide a sterile medium for the administration of compatible intravenous medications.

• Common Indications:

  • Isotonic Dehydration: Replacement of water and salt loss due to hemorrhage, severe vomiting, or diarrhea.

  • Extracellular Fluid Replacement: Maintaining blood volume during surgery or in shock states.

  • Initial Management of Hyponatremia: Treating sodium depletion.

  • Wound Irrigation: Used as a sterile wash for wounds, burns, or during surgical procedures.

  • Drug Diluent: The standard carrier for the infusion of numerous antibiotics, analgesics, and emergency medications.

• Administration: Intravenous infusion.

  • Dose: The volume and rate are highly dependent on the patient’s age, weight, and clinical condition (e.g., cardiac or renal status).

• Pharmacist’s Note: Monitor for Fluid Overload. As a professional, you must ensure caution in patients with hypertension, congestive heart failure, or peripheral edema. Prolonged or rapid infusion of 0.9% NaCl can lead to hypernatremia and hyperchloremic metabolic acidosis.

Therapeutic Category

• Primary Classification: Electrolyte Solutions.

• Pharmacological Class: Isotonic Crystalloid.

• ATC Code: B05BB01.

Pharmacological Mechanism: Isotonic Volume Expansion

Sodium Chloride 0.9% is considered "Normal" because its osmolarity ($308\text{ mOsm/L}$) closely approximates the osmolarity of human plasma:

1. Isotonic Balance: Because it is isotonic, the fluid remains primarily in the extracellular compartment (interstitial and intravascular space) rather than moving into the cells.

2. Pressure Maintenance: The infusion increases the intravascular volume, which in turn raises venous return and cardiac output, stabilizing blood pressure.

3. Electrolyte Supply: It provides $154\text{ mEq/L}$ of both Sodium ($Na^+$) and Chloride ($Cl^-$) ions, which are essential for maintaining the osmotic pressure of the extracellular fluid.

B2B Technical Specifications

Approx. Rs 10.69 / StripGet Latest Price

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Each Ml Contains: Dexamethasone Sodium Phosphate IP Eq. To Dexamethasone 4 Mg + Methyl Paraben IP (As A Preservative) 0.18% W/v + Propyl Paraben IP (As A Preservative) 0.02% W/v + Water For Injection IP Q.s
DEXATORE 2ml (Dexamethasone Sodium Phosphate Injection IP)

Healthy Inc offers DEXATORE 2ml, a fast-acting Corticosteroid and potent Glucocorticoid injectable. Containing 4 mg of Dexamethasone Sodium Phosphate per ml (8 mg total per 2ml ampoule), DEXATORE is a clinical cornerstone for the management of severe inflammatory, allergic, and autoimmune conditions. It is a critical-care priority for treating Anaphylaxis, Cerebral Edema, Acute Asthma exacerbations, and providing supportive therapy in Septic Shock. As a specialized Indian export partner, we supply this high-efficacy emergency medicine to hospital networks and trauma centers across global pharmaceutical markets.

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

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

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

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

Available strengths and quality? We supply DEXATORE in 2ml ampoules providing a total dose of 8mg (4mg/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. DEXATORE is Zone IVb stability-tested. We utilize neutral USP Type I glass ampoules and specialized export-grade secondary packaging to prevent chemical degradation during international transit to high-temperature regions.

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

Small-volume or mixed orders? We specialize in mixed-container consolidation, allowing you to combine DEXATORE with other therapeutic categories (such as antibiotics, PPI injectables, or emergency critical care medicines) in a single, cost-effective shipment 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 40.82 / VialGet Latest Price

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Each Vial Contains :Ceftriaxone Sodium I.P. (Sterile) Eq. To Anhydrous Ceftriaxone 250MG + Sulbactam Sodium 125 MG & Sterile Water For Injection I.P 5 Ml. Elsewhere And Packed With In This Combi - Pack)
MONODOSE-SB 375 mg Injection (Ceftriaxone 250 mg & Sulbactam 125 mg)

Healthy Inc offers MONODOSE-SB 375, a specialized low-dose Beta-lactam / Beta-lactamase Inhibitor combination. This formulation pairs Ceftriaxone, a potent third-generation cephalosporin, with Sulbactam, a beta-lactamase inhibitor that protects Ceftriaxone from enzymatic degradation. The 375 mg strength is a clinical priority for Pediatric Infections, including Neonatal Septicemia, Bronchopneumonia, and Urinary Tract Infections (UTI) caused by resistant organisms. As a specialized Indian export partner, we supply this essential pediatric anti-infective to neonatal units and pediatric hospitals in global pharmaceutical markets.

• Overcoming Resistance: Sulbactam expands the spectrum of Ceftriaxone to include many beta-lactamase-producing strains of H. influenzae, S. aureus, and Klebsiella species, ensuring clinical success in empirical pediatric therapy.

• Manufacturing: Produced in associated WHO-GMP certified sterile facilities. The dry powder for injection is manufactured under strict environmental controls to ensure 100% sterility and high molecular stability.

• Climate Stability: Validated for Zone IVb (Hot/Humid) conditions; the dry powder form ensures potency and a long shelf life across the tropical climates of Africa, LATAM, and SEA markets.

• Regulatory Support: Full technical documentation available, including CTD/eCTD Dossiers, to facilitate the registration of specialized pediatric anti-infectives.

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

Available strengths and packaging? We supply MONODOSE-SB in the 375 mg (250 mg + 125 mg) strength, as well as 1.5 g (1000 mg + 500 mg) for adult use. The 375 mg vial is typically supplied with a sterile diluent (Sterile Water for Injection) for precise reconstitution.

Support for tropical export? Yes. MONODOSE-SB 375 is Zone IVb stability-tested. We utilize neutral USP Type I glass vials and moisture-resistant secondary packaging to ensure product integrity during international transit to high-temperature regions.

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

Small-volume or mixed orders? We specialize in mixed-container consolidation, allowing you to combine MONODOSE-SB 375 with other pediatric essentials (such as Amikacin, Metoclopramide, or pediatric IV fluids) in a single, cost-effective shipment.

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