
Meropenem Iv Infusion Suppliers & Bulk Manufacturers
Available Forms: Powder for Reconstitution
Available Strengths: 500 mg, 1 g, 2 g in vials
Reference Brands: Merrem (US & EU)
Category: Antibiotics
Meropenem IV infusion is available in Powder for Reconstitution and strengths such as 500 mg, 1 g, 2 g in vials. 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 infusion 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 infusion 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 infusion is approved in the EU and US for severe bacterial infections including pneumonia, urinary tract infections, and intra-abdominal sepsis. In the EU, brands like Merrem are regulated by EMA with dossiers demonstrating safety, efficacy, and manufacturing standards. In the US, FDA approval relies on extensive clinical data; generic options are available. Both regions require detailed dossiers including clinical trial results, quality assurance, and pharmacovigilance plans for approval and ongoing safety monitoring. Due to its critical role in combatting resistant bacteria, strict prescribing and monitoring guidelines are enforced. For expert help with regulatory dossiers, compliance, and registration, visit PharmaTradz. We enable seamless market access aligned with European and US standards.
The Trade Mark owner has been correctly identified under the heading Manufacturer / TM Owner as required by the Act.
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