Amoxicillin Trihydrate Tablets And Suspension Suppliers & Bulk Manufacturers
Available Forms: Oral Tablets and Suspension
Available Strengths: 500 mg and 875 mg, Suspension: 50 mg/mL
Reference Brands: Amoxil(US & EU) and generic brands
Category:
Veterinary Product
Amoxicillin tri hydrate tablets and suspension inhibit bacterial cell wall synthesis by targeting penicillin-binding proteins, leading to bacterial death. They treat various infections like respiratory, urinary, and skin. Benefits include broad-spectrum activity, rapid symptom relief, prevention of complications, and promoting recovery when used appropriately under veterinary or medical guidance.
Amoxicillin Trihydrate tablets and suspension is available in Oral Tablets and Suspension
and strengths such as 500 mg and 875 mg, Suspension: 50 mg/mL.
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, Amoxicillin Trihydrate tablets and suspension 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) |
Amoxicillin Trihydrate tablets and suspension 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:
Amoxicillin tri hydrate tablets and suspension are approved in both the US and EU, supported by dossiers demonstrating safety, efficacy, and manufacturing quality in accordance with GMP standards. In the US, FDA approval involves clinical evaluation and safety data, while in the EU, CE marking certifies conformity with veterinary and human 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 regulatory updates, visit Pharmatradz. Ensuring compliance guarantees access to safe, effective amoxicillin formulations for human and veterinary use worldwide—supporting infection treatment and disease prevention efforts.
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