Meropenem Iv Suppliers & Bulk Manufacturers
Available Forms: Intravenous (IV)
Available Strengths: 500 mg, 1 g, 2 g per vial
Reference Brands: Merrem (US & EU)
Category:
Antibiotics
Meropenem inhibits bacterial cell wall synthesis by binding to penicillin-binding proteins, causing bacteria to lyses and die. It offers broad-spectrum activity against resistant gram-negative and gram-positive bacteria, including Pseudomonas. Benefits include rapid bactericidal effect, good tissue penetration, and suitability for severe, life-threatening infections in hospital settings.
Meropenem iv is available in Intravenous (IV)
and strengths such as 500 mg, 1 g, 2 g per vial.
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, Meropenem iv 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) |
Meropenem iv 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:
Meropenem IV is approved in the EU and US for severe bacterial infections, including pneumonia, meningitis, and intra-abdominal infections. In the EU, brands like Merrem 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 generic options available. Both regions require detailed dossiers, including clinical trial results, quality control, and pharmacovigilance plans for approval and safety monitoring. Due to its critical role in fighting resistant infections, strict prescribing controls and safety guidelines are enforced. For regulatory support and dossier assistance, visit PharmaTradz. We support seamless market access while ensuring adherence to European and US standards.
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