
Paracetamol (Acetaminophen) Tablets Suppliers & Bulk Manufacturers
Available Forms: Oral Tablets
Available Strengths: 500 mg, 650 mg, 1000 mg (US), 500 mg
Reference Brands: Tylenol(US)
Category: Analgesic
Paracetamol (Acetaminophen) tablets is available in Oral Tablets and strengths such as 500 mg, 650 mg, 1000 mg (US), 500 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, Paracetamol (Acetaminophen) tablets 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) |
Paracetamol (Acetaminophen) tablets 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) is widely approved in the EU and US for pain and fever relief. In the EU, brands like Panadol are regulated by EMA, supported by dossiers demonstrating safety, efficacy, and manufacturing quality. In the US, FDA approval is based on extensive clinical data, with numerous generic options available. Both regions require detailed dossiers for initial approval and continuous pharmacovigilance. For expert assistance with regulatory dossiers, compliance, and registration, visit PharmaTradz. We support efficient market access for paracetamol, ensuring adherence to European and American standards for safe, effective analgesic and antipyretic therapy, helping you navigate complex regulatory landscapes seamlessly.
The Trade Mark owner has been correctly identified under the heading Manufacturer / TM Owner as required by the Act.
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