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Tenofit EM Tablet

Composition : Emtricitabine (200mg) + Tenofovir disoproxil fumarate (300mg) Tablet

Dosage Form : Tablet

Packaging Type : in a Bottle

Packaging : 30 Tablets

Price : ₹1/-

Tenofit EM Tablet contains Emtricitabine 200mg and Tenofovir Disoproxil Fumarate 300mg, a globally recommended fixed-dose antiretroviral combination used as a first-line therapy in the management of HIV-1 infection. This dual-action formulation works by inhibiting viral reverse transcriptase, effectively suppressing HIV replication and reducing viral load.

This combination is widely used as part of standard antiretroviral therapy regimens and is also approved for HIV pre-exposure prophylaxis (PrEP). Its proven efficacy, favorable resistance profile, and once-daily dosing make it a preferred option in long-term HIV management programs.

For hospitals, ART centers, and institutional suppliers, Tenofit EM Tablet is a high-demand antiretroviral medicine, consistently required for government HIV programs, private infectious disease clinics, and specialty care hospitals. Ongoing treatment protocols ensure continuous procurement and stable market movement.

Adding Tenofit EM Tablet to your portfolio strengthens your HIV and antiretroviral therapy segment, enabling opportunities in hospital supply, national health tenders, export markets, and third-party manufacturing. Its essential role in HIV treatment and prevention makes it a strategically important and commercially valuable product for pharmaceutical distributors.


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About the Product

Tenofit EM Tablet contains Emtricitabine 200mg and Tenofovir Disoproxil Fumarate 300mg, a globally recommended fixed-dose antiretroviral combination used as a first-line therapy in the management of HIV-1 infection. This dual-action formulation works by inhibiting viral reverse transcriptase, effectively suppressing HIV replication and reducing viral load.

This combination is widely used as part of standard antiretroviral therapy regimens and is also approved for HIV pre-exposure prophylaxis (PrEP). Its proven efficacy, favorable resistance profile, and once-daily dosing make it a preferred option in long-term HIV management programs.

For hospitals, ART centers, and institutional suppliers, Tenofit EM Tablet is a high-demand antiretroviral medicine, consistently required for government HIV programs, private infectious disease clinics, and specialty care hospitals. Ongoing treatment protocols ensure continuous procurement and stable market movement.

Adding Tenofit EM Tablet to your portfolio strengthens your HIV and antiretroviral therapy segment, enabling opportunities in hospital supply, national health tenders, export markets, and third-party manufacturing. Its essential role in HIV treatment and prevention makes it a strategically important and commercially valuable product for pharmaceutical distributors.


Some patients may experience nausea, diarrhea, headache, dizziness, fatigue, or abdominal discomfort. Rarely, kidney dysfunction, decrease in bone mineral density, or lactic acidosis may occur with long-term use.

Tenofit EM Tablet is indicated for the treatment of HIV-1 infection as part of combination antiretroviral therapy. It is also used for pre-exposure prophylaxis (PrEP) to reduce the risk of HIV infection in high-risk individuals, as advised by a healthcare professional.

Use strictly under medical supervision. Regular monitoring of kidney function and bone health is recommended. Do not discontinue therapy abruptly without consulting a doctor, as this may worsen HIV infection or lead to resistance.

Store in a cool, dry place below 25°C, away from moisture and direct sunlight. Keep out of reach of children.

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Regulatory Compliance & Professional Verification

This catalog is a digital representation of the Cafoli Lifecare portfolio and is intended for use by authorized pharmaceutical distributors and PCD franchise partners.

  • No Consumer Sale: We do not entertain retail inquiries or direct sales to patients.
  • Information Accuracy: While we strive for accuracy, product availability, packaging, and regulatory status may change based on CDSCO guidelines and state-specific drug laws.
  • Medical Advice: Patients are strictly advised not to self-medicate or use this information for treatment. Always consult a qualified medical practitioner.
  • Licensing: All business associations are subject to the submission of valid GST and Drug License (DL) documentation.

Strategic Advisory

Ms. Shiwani Dhiman

VP-Strategic Outreach & Engagement

Ms. Shiwani specializes in market outreach and strategic partnership orchestration for entrepreneurs building scalable PCD Pharma Franchise models.

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