Tetracycline Tablets/Capsules Suppliers & Bulk Manufacturers
Available Forms: Tablet/Capsules
Available Strengths: 250 mg, 500 mg
Reference Brands: Sumycin(US)
Category:
Antibiotics
Tetracycline inhibits bacterial protein synthesis by binding to the 30S ribosomal subunit, preventing aminoacyl-tRNA attachment. It effectively treats respiratory, urinary, and skin infections. Benefits include broad-spectrum activity, rapid bacterial eradication, and oral administration, making it a reliable option for managing various bacterial infections.
Tetracycline tablets/Capsules is available in Tablet/Capsules
and strengths such as 250 mg, 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, Tetracycline tablets/Capsules 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) |
Tetracycline tablets/Capsules 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:
Tetracycline tablets are approved in the EU and US for respiratory, urinary, and skin bacterial infections. In the EU, brands like Sumycin are regulated by EMA, supported by dossiers demonstrating safety, efficacy, and manufacturing standards. In the US, FDA approval relies on extensive clinical data; generic formulations are available. Both regions require detailed dossiers, including clinical trial results, manufacturing practices, and pharmacovigilance plans for approval and ongoing safety monitoring. For expert assistance with regulatory dossiers, compliance, and registration, visit PharmaTradz. We support seamless market access for tetracycline, ensuring adherence to European and US standards for safe, effective antimicrobial therapy.
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