Lamivudine & Zidovudine tablets

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Product Composition & Strength

We supply this product in the internationally standardized Fixed-Dose Combination (FDC) required for therapeutic compliance.

Active IngredientStrength (per Tablet)Primary Clinical Function
Lamivudine (3TC) IP/BP/USP150 mgThe Chain Terminator: High potency, low toxicity.
Zidovudine (AZT) IP/BP/USP300 mgThe Foundation: Proven efficacy in preventing replication.
ExcipientsPharma GradeThe Matrix: Ensures stability of the sensitive FDC.

Description

Lamivudine & Zidovudine tablets

Lamivudine & Zidovudine Tablets (150 mg / 300 mg)

Healthy Inc is a specialized global supplier and exporter of advanced infectious disease, immunology, and public health therapeutics. We provide ultra-high-purity, kinetically stable Lamivudine and Zidovudine FDC Tablets, manufactured in WHO–GMP certified, high-precision antiretroviral manufacturing facilities. This “Nucleoside Reverse Transcriptase Inhibitor (NRTI) Combination” is a massive-volume strategic export to National AIDS Control Organizations, global health NGOs, and international B2B distributors, serving as the globally preferred backbone for the long-term management of HIV-1 infection.

Product Overview

This formulation operates as a “Genetic Chain Terminator.” It ensures patient safety by blocking the virus’s ability to convert its RNA into DNA, physically preventing it from integrating into the host’s immune cells.

  • Mechanism 1 (Nucleoside Mimicry): Both Lamivudine and Zidovudine are physically engineered to resemble natural deoxynucleotides. The HIV enzyme, Reverse Transcriptase, chemically mistakes these drugs for actual DNA building blocks.

  • Mechanism 2 (Chain Termination): Once the enzyme incorporates the drug into the growing viral DNA strand, it physically lacks the chemical “hook” (3′-OH group) needed to attach the next block. This chemically and physically Terminates the DNA Chain.

  • Mechanism 3 (Dual-Synergy): By using two different NRTIs, the treatment physically increases the barrier to resistance, chemically ensuring a more robust suppression of the viral load than monotherapy.


Product Composition & Strength

We supply this product in the internationally standardized Fixed-Dose Combination (FDC) required for therapeutic compliance.

Active IngredientStrength (per Tablet)Primary Clinical Function
Lamivudine (3TC) IP/BP/USP150 mgThe Chain Terminator: High potency, low toxicity.
Zidovudine (AZT) IP/BP/USP300 mgThe Foundation: Proven efficacy in preventing replication.
ExcipientsPharma GradeThe Matrix: Ensures stability of the sensitive FDC.

Technical & Logistics Specifications

  • HS Code: 3004.90.99 (Medicaments acting on infectious diseases / Antivirals)

  • CAS Numbers: 134678-17-4 (Lamivudine) / 30516-87-1 (Zidovudine)

  • Dosage Form: Oral Tablet (Film-Coated)

  • Packaging: 10 or 60 Tablets per Bottle/Blister. We utilize high-density induction-sealed bottles or Alu-Alu blisters to physically prevent moisture ingress, ensuring 36-month stability in Zone IVb tropical climates.


Manufacturing Authority & Compliance

  • ARV Specialized Line: HIV medications require the highest level of cross-contamination control. Our manufacturing process utilizes Dedicated High-Containment Facilities, physically ensuring that no other drug particles chemically interfere with the ARV matrix.

  • Bioequivalence Verification: We utilize Comparative Dissolution Profiling, physically ensuring our FDC is chemically bioequivalent to the innovator brand—a critical factor for NGO and Government tender qualification.

  • Photo-Stability: Zidovudine is physically sensitive to light. We utilize Opaque Film Coating and light-resistant packaging, chemically ensuring the drug remains potent until the point of ingestion.

Primary Indications

  • HIV/AIDS Management: Part of a multi-drug regimen for the treatment of HIV-1 Infection.

  • Occupational Safety: Used in Post-Exposure Prophylaxis (PEP) following potential needle-stick or sexual exposure.

  • Maternal Health: Prevention of Mother-to-Child Transmission (PMTCT) during pregnancy and delivery.

Usage Instructions

  • Dosage: Typically one tablet twice daily (every 12 hours).

  • Administration: Swallow the tablet physically whole with or without food.

  • Consistency: Adherence is physically critical. Missing doses chemically allows the virus to replicate and physically increases the risk of Drug Resistance.

  • Monitoring: Patients must physically undergo regular CD4 Count and Viral Load Testing to chemically assess the treatment’s success.

Safety Warning: For Professional Use Only. Hematologic Note: Zidovudine may physically cause Anemia or Neutropenia; monitor blood counts chemically. Lactic Acidosis: Rare but severe physical risk of lactic acidosis and hepatic steatosis. Contraindication: Do not use in patients with severe anemia, very low neutrophil counts, or known hypersensitivity to Lamivudine or Zidovudine.


Global Export & Contract Manufacturing

Healthy Inc is a premier Antiretroviral and Public Health Pharmaceutical Exporter in India. As a verified Medicine Supplier in Mumbai, we offer flexible Third Party Manufacturing (Contract Manufacturing) for high-volume ARV FDCs. Whether you are a National Ministry of Health in Africa or a B2B Pharma Marketplace partner in the CIS or SE Asia, we ensure secure, WHO-GMP compliant delivery.

Commercial Inquiries:

WhatsApp/Call: +91 7710003340

Email: info@healthyinc.co.in