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Description
PRODUCT DESCRIPTION:
Tenofovir Disoproxil Fumarate (TDF) Tablets 300 MG is a globally recognized nucleotide reverse transcriptase inhibitor (NRTI), used extensively in first-line antiretroviral therapy (ART) for HIV-1 infection and chronic Hepatitis B (HBV).
As a once-daily oral medication, TDF plays a critical role in reducing viral load and improving immune function. With its proven safety profile and WHO-preferred status, TDF is a mainstay in global HIV and HBV programs.
Our formulations are produced in WHO-GMP and regulatory-compliant facilities, making them suitable for global health tenders, humanitarian programs, and public health initiatives.
Formulation & Presentation:
- Dosage Form: Tablets
- Presentation: Available in Blister Pack or HDPE Bottle (As per market requirement)
- Available Strengths:
- Tenofovir Disoproxil Fumarate Tablets: 300 MG
- Route of Administration: Oral (As per physician’s discretion or therapeutic indication)
Therapeutic Indications:
- Treatment of HIV-1 infection, in combination with other antiretrovirals
- Chronic Hepatitis B infection
- Used in post-exposure prophylaxis (PEP) in high-risk settings
- Core component in pre-exposure prophylaxis (PrEP) when used with Emtricitabine
Side Effects:
- COMMON:
- Nausea
- Diarrhea
- Fatigue
- Headache
- Dizziness
- Rash
- SERIOUS (RARE):
- Lactic acidosis
- Severe hepatomegaly with steatosis
- Renal toxicity (Fanconi syndrome, proximal tubulopathy)
- Decreased bone mineral density
- Immune reconstitution syndrome
- PRECAUTIONS:
- Monitor renal function periodically in long-term therapy
- Use cautiously in patients with osteoporosis or bone risk factors
- Avoid use with other nephrotoxic agents
- Should not be used as monotherapy for HIV
- Monitor liver enzymes in HBV co-infection, especially on discontinuation
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TECHNICAL INFORMATION
Product Specifications:
- HSN Code: To be assigned per international classification standards
- Weight: Approx. 40g per Carton (With Packaging)
- Dimensions: (15x1x8 CMS)
- Shelf Life (Subject To Country Specific Guidelines): 24 to 36 months from date of manufacture or as per label specifications
- Storage: Store below 25°C. Protect from moisture, direct sunlight & children.
Regulatory Status & Supply Information:
- Regulatory Status: WHO-GMP Complaint Manufacturing. Further certifications available on request
- Exports Ready Dossiers: Dossier Available (CTD/eCTD formats)
- Stability: Zone IVB Compliant
- MOQ: Negotiable. Based on market & registration status
- Export Options: Available for private label, institutional supply, or branded export
Who Should Source This Product?
- HIV/AIDS programs run by NGOs, governments, and global donors (e.g., PEPFAR, Global Fund)
- Public health procurement agencies and antiretroviral access programs
- Hospital chains and infectious disease centers managing HIV and HBV cases
- Distributors aligned with national ART rollouts
- Emergency stockpiling agencies ensuring access to essential ARVs in resource-limited regions
Why Source from PHARMET?
- Oncology-focused distributors in emerging and regulated markets
- Government tenders and hospital procurement departments
- Cancer foundations and treatment support NGOs
- Pharma wholesalers serving LATAM, Africa, Southeast Asia
- Regulatory-compliant buyers seeking dossier-backed hormone therapies
CONTACT DETAILS:
- E-MAIL: hello@pharmet.io
- Phone/WhatsApp Number: +91 9999091881
- Website: www.pharmet.io
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