Atazanavir & Ritonavir Suppliers & Bulk Manufacturers
Available Forms: Tablets
Available Strengths: 300 mg Atazanavir + 100 mg Ritonavir
Reference Brands: Evotaz®(US)
Category: Anti Viral
Atazanavir & Ritonavir is available in Tablets and strengths such as 300 mg Atazanavir + 100 mg Ritonavir. 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, Atazanavir & Ritonavir 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) |
Atazanavir & Ritonavir 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: Atazanavir & Ritonavir Tablets are a fixed-dose antiretroviral combination used in the management of HIV-1 infection, with Ritonavir boosting Atazanavir’s effectiveness. Available in a 300 mg + 100 mg formulation, this once-daily therapy is WHO-recommended and USFDA-approved. On PharmaB2B platforms, global buyers can connect with GMP-certified manufacturers for bulk procurement of quality-assured Atazanavir/Ritonavir tablets. Ideal for hospitals, NGOs, government tenders, and HIV treatment programs, PharmaB2B simplifies sourcing of affordable, compliant ARVs. Partner with reliable suppliers to support uninterrupted access to essential HIV care in both regulated and emerging markets.
The Trade Mark owner has been correctly identified under the heading Manufacturer / TM Owner as required by the Act.
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