Pegylated Interferon Alpha-1A Suppliers & Bulk Manufacturers
Available Forms: Injection
Available Strengths: 120 mcg, 150 mcg, 180 mcg
Reference Brands: Pegasys® (US & EU), PegIntron® (EU)
Category: Hepatitis
Pegylated Interferon Alpha-1a is available in Injection and strengths such as 120 mcg, 150 mcg, 180 mcg. 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, Pegylated Interferon Alpha-1a 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) |
Pegylated Interferon Alpha-1a 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.
The Trade Mark owner has been correctly identified under the heading Manufacturer / TM Owner as required by the Act.
Product Description: PegIntron® is a pegylated interferon alpha-2b injection used for treating chronic Hepatitis C infection. It delivers a sustained antiviral effect by stimulating the immune response against the virus. Available in prefilled syringes with strengths of 120 mcg, 150 mcg, and 180 mcg, PegIntron® is administered once weekly via subcutaneous injection, typically dosed at 1.5 mcg/kg. Often combined with ribavirin, it is manufactured under EU-GMP and USFDA standards. PegIntron® is widely used in hospital tenders, B2B supply, and licensing with comprehensive regulatory dossiers to support market entry in EU and US.
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