Fenbendazole Granules Or Powder Suppliers & Bulk Manufacturers
Available Forms: Granules/powder
Available Strengths: 222 mg per gram (22.2%)
Reference Brands: Panacur(US & EU)
Category:
Veterinary Product
Fenbendazole granules or powder inhibit worm microtubule formation by binding to tubulin, disrupting nutrient absorption and leading to parasite death. It effectively treats gastrointestinal worms in animals, reducing infection spread, relieving symptoms, and improving overall health, making it a widely used broad-spectrum anthelmintic.
Fenbendazole Granules or powder is available in Granules/powder
and strengths such as 222 mg per gram (22.2%).
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, Fenbendazole Granules or powder 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) |
Fenbendazole Granules or powder 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:
Fenbendazole granules and powder are approved in the EU and US for veterinary use, supported by dossiers demonstrating safety, efficacy, and manufacturing quality in line with GMP standards. In the US, FDA approval involves extensive clinical data and safety evaluations, while in the EU, CE marking certifies conformity with veterinary medicinal regulations. These products undergo validation, stability testing, and quality audits, with comprehensive documentation including safety profiles, clinical trial data, and manufacturing practices. For licensing procedures, approved dossiers, and the latest regulatory updates, visit Pharmatradz. Ensuring compliance guarantees access to safe, effective anthelmintics to treat parasitic infections in animals worldwide.
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