
Dobutamine Suppliers & Bulk Manufacturers
Available Forms: Intravenous (IV) Injection
Available Strengths: 12.5 mg/mL
Reference Brands: Dobutrex(US), Dobutamina Hameln, Dobutamine Accord, Dobutamine Fresenius Kabi(EU)
Category: Critical Care
Dobutamine is available in Intravenous (IV) Injection and strengths such as 12.5 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, Dobutamine 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) |
Dobutamine 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: Dobutamine is a fast-acting inotropic agent used to treat acute heart failure and cardiogenic shock by enhancing cardiac output. Administered via intravenous infusion, it acts on beta-1 adrenergic receptors to improve myocardial contractility. Dobutamine is commonly available in 12.5 mg/mL concentration, supplied in 250 mg/20 mL and 500 mg/40 mL vials or ready-to-use infusion bags. Brands like Dobutamina Hameln and Dobutamine Fresenius are well-recognized in the EU, with various generics available in the US. Dobutamine is a critical care medication procured by hospitals, ICUs, and emergency departments, often listed in institutional tenders and group purchasing organizations.
The Trade Mark owner has been correctly identified under the heading Manufacturer / TM Owner as required by the Act.
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