Dexmedetomidine bulk supplier for pharma manufacturers

Dexmedetomidine Suppliers & Bulk Manufacturers

Available Forms: Intravenous (IV) Infusion/Injection

Available Strengths: 100 mcg/mL

Reference Brands: Precedex(US); Dexdor(EU)

Category: Critical Care

Dexmedetomidine is available in Intravenous (IV) Infusion/Injection and strengths such as 100 mcg/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, Dexmedetomidine 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)

Dexmedetomidine 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.

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Product Description: Dexmedetomidine is a highly selective alpha-2 adrenergic agonist used for sedation in ICU and surgical settings without causing respiratory depression. Available as a 100 mcg/mL concentrate in 2 mL and 4 mL vials, and as ready-to-use infusions (4 mcg/mL in 50 mL and 100 mL), it ensures flexible dosing and efficient workflow. In the US, Precedex by Pfizer and generic alternatives are widely used. The EU features Dexdor (Orion), Accord, and B. Braun formulations. Dexmedetomidine is a critical care drug frequently procured via pharma B2B platforms for operating rooms, ICUs, and procedural sedation in institutional healthcare settings.

Frequently Asked Questions

Yes, Dexmedetomidine is available with DMF and other regulatory documents such as COA and MSDS. These can be provided upon request for qualified buyers.

Absolutely. Sample requests are accepted for formulation trials and quality checks. Please submit an enquiry to initiate the process.

Our manufacturing partners are GMP-certified and comply with ISO and WHO standards, ensuring global quality benchmarks.

Lead times vary based on quantity and destination, but most orders are fulfilled within 1–3 weeks. Express shipping options are available.

Yes, Dexmedetomidine is exported to over 30 countries across Asia, Africa, Europe, and Latin America. We support documentation for customs and regulatory clearance.

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