Paracetamol (Acetaminophen) Granules Suppliers & Bulk Manufacturers
Available Forms: Granules for reconstitution; Bulk powder
Available Strengths: High-purity granules or powder with concentrations usually 50% or higher
Reference Brands: Generic formulations
Category:
Active Pharmaceutical Ingredient
Paracetamol (acetaminophen) API granules inhibit prostaglandin synthesis in the brain, reducing pain and fever. They support rapid formulation development for oral suspensions and tablets. Benefits include effective, quick relief for mild to moderate pain, reduced fever, and versatile use in pharmaceutical manufacturing for safe, reliable fever and pain management.
Paracetamol (Acetaminophen) Granules is available in Granules for reconstitution; Bulk powder
and strengths such as High-purity granules or powder with concentrations usually 50% or higher.
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, Paracetamol (Acetaminophen) Granules is supplied in
bulk quantities with complete regulatory support including DMF, COA, and MSDS.
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Technical Specifications & Supply Details
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| 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) |
Paracetamol (Acetaminophen) Granules 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:
Paracetamol (acetaminophen) API granules are regulated in the EU and US, supported by dossiers demonstrating safety, efficacy, and manufacturing quality in compliance with GMP standards. In the US, FDA approval requires extensive validation, safety testing, and GMP compliance. In the EU, CE marking certifies conformity with MDR standards. These granules undergo validation, stability testing, and audits, with comprehensive documentation including safety profiles, clinical data, and manufacturing practices. For licensing procedures, approved dossiers, and the latest regulatory updates, visit Pharmatradz. Ensuring compliance guarantees access to high-quality paracetamol API granules for pharmaceutical manufacturing, supporting safe, effective formulations for pain and fever management worldwide.
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