 
				            Human Normal Immunoglobulin Suppliers & Bulk Manufacturers
Available Forms: (IVIG) & (SCIG)
Available Strengths: IVIG: 5%, 10%, 16%, 20%; SCIG: 20%
Reference Brands: Privigen®, Gamunex-C® (EU & US)
Category: Hepatitis
Human Normal Immunoglobulin is available in (IVIG) & (SCIG) and strengths such as IVIG: 5%, 10%, 16%, 20%; SCIG: 20%. 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, Human Normal Immunoglobulin 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) | 
Human Normal Immunoglobulin 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: Human Normal Immunoglobulin Injection is a sterile, purified preparation of pooled human plasma antibodies used for passive immunization and immune support. It treats immunodeficiency disorders, autoimmune diseases, and certain infections by providing broad-spectrum antibodies. Available as intravenous (IVIG) or subcutaneous (SCIG) formulations with concentrations typically ranging from 5% to 20%. Manufactured under stringent EU-GMP and USFDA standards, it is ideal for hospital supply, tender bids, and B2B partnerships. Complete regulatory dossiers and batch-release documentation support rapid registration and distribution in global and regulated markets.
The Trade Mark owner has been correctly identified under the heading Manufacturer / TM Owner as required by the Act.
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