Velpatasvir + Sofosbuvir bulk supplier for pharma manufacturers

Velpatasvir + Sofosbuvir Suppliers & Bulk Manufacturers

Available Forms: Tablet

Available Strengths: Sofosbuvir - 400 mg + Velpatasvir - 100 mg

Reference Brands: Epclusa(US & EU)

Category: Anti Viral

Velpatasvir + Sofosbuvir is available in Tablet and strengths such as Sofosbuvir - 400 mg + Velpatasvir - 100 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, Velpatasvir + Sofosbuvir 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)

Velpatasvir + Sofosbuvir 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.

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Product Description: Epclusa is a once-daily, fixed-dose combination of Sofosbuvir 400 mg and Velpatasvir 100 mg, approved by the FDA and EMA for the treatment of chronic hepatitis C virus (HCV) infection across all six genotypes. This pan-genotypic regimen offers a high sustained virologic response (SVR) rate of over 95%, making it a preferred choice for both treatment-naïve and previously treated patients. Epclusa is suitable for use with or without ribavirin, depending on liver disease status. Its simplified, one-pill-daily format improves adherence and outcomes. It is also available for pediatric patients aged 3 years and older in tablet and granule forms.

Frequently Asked Questions

Yes, Velpatasvir + Sofosbuvir is available with DMF and other regulatory documents such as COA and MSDS. These can be provided upon request for qualified buyers.

Absolutely. Sample requests are accepted for formulation trials and quality checks. Please submit an enquiry to initiate the process.

Our manufacturing partners are GMP-certified and comply with ISO and WHO standards, ensuring global quality benchmarks.

Lead times vary based on quantity and destination, but most orders are fulfilled within 1–3 weeks. Express shipping options are available.

Yes, Velpatasvir + Sofosbuvir is exported to over 30 countries across Asia, Africa, Europe, and Latin America. We support documentation for customs and regulatory clearance.

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