Tenofovir & Emtricitabine Suppliers & Bulk Manufacturers
Available Forms: Tablet
Available Strengths: Tenofovir DF 300 mg + Emtricitabine 200 mg
Reference Brands: Truvada®(US/EU)
Category: Anti Viral
Tenofovir & Emtricitabine is available in Tablet and strengths such as Tenofovir DF 300 mg + Emtricitabine 200 mg. Sourced from GMP-certified and ISO-compliant manufacturers, this API meets global pharmacopeia standards (USP/EP/JP as applicable). Ideal for pharmaceutical formulation and commercial manufacturing, Tenofovir & Emtricitabine is supplied in bulk quantities with complete regulatory support including DMF, COA, and MSDS.
| Technical Specifications & Supply Details | |
|---|---|
| Lead Time | 7 to 60 days (depending on batch size & schedule) |
| MOQ | As per manufacturer’s batch size |
| COA | Available with every batch |
| Regulatory Dossier / DMF | Available upon request |
| Export Documentation | FSC, COA, Manufacturing License, Product Permission |
| Standards | IP, BP, USP |
| Certifications | WHO-GMP, EU-GMP, USFDA (as applicable) |
Tenofovir & Emtricitabine can be exported to over 30 countries across Asia, Africa, Europe, and Latin America. Flexible packaging, competitive pricing, and a verified supplier network make Pharmatradz a trusted sourcing partner for pharmaceutical companies and contract manufacturers worldwide.
Product Description: Tenofovir & Emtricitabine Tablets (300 mg/200 mg), marketed under brands like Truvada®, Tenvir-EM®, and Ricovir-EM®, are WHO-recommended antiretrovirals used for both HIV-1 treatment and pre-exposure prophylaxis (PrEP). This fixed-dose, once-daily combination offers high efficacy with a strong safety profile. On PharmaB2B platforms, global buyers, NGOs, and procurement agencies can source WHO-GMP and USFDA-approved formulations in bulk from trusted manufacturers. Ideal for HIV prevention programs, public health supply chains, and international tenders, Tenofovir + Emtricitabine supports global access to affordable, life-saving HIV care. Partner with reliable suppliers for consistent, quality-assured ARV supply.
The Trade Mark owner has been correctly identified under the heading Manufacturer / TM Owner as required by the Act.
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