Tranexamic Acid Suppliers & Bulk Manufacturers
Available Forms: Tablets
Available Strengths: 500 mg, 650 mg
Reference Brands: Lysteda®(US)
Category: Critical Care
Tranexamic Acid is available in Tablets and strengths such as 500 mg, 650 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, Tranexamic Acid 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) |
Tranexamic Acid 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.
The Trade Mark owner has been correctly identified under the heading Manufacturer / TM Owner as required by the Act.
Product Description: Tranexamic Acid is an antifibrinolytic agent used to reduce or prevent excessive bleeding in surgical, trauma, and gynecological settings. Available in IV and oral forms, it is commonly supplied as 100 mg/mL injection or 500 mg tablets. Leading brands include Cyklokapron® (Pfizer), Lysteda® (Ferring), and Exacyl® (Sanofi). Widely adopted in both emergency medicine and elective surgeries, tranexamic acid helps stabilize clots and minimize transfusion needs. Pharma B2B platforms provide access to GMP-certified tranexamic acid products in bulk quantities, supporting hospitals, surgical centers, and emergency care providers with reliable global sourcing and compliance with US and EU pharmaceutical standards.
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