Teduglutide 5 mg vial Suppliers & Bulk Manufacturers
Available Forms: Injection
Available Strengths: 5 mg vial
Reference Brands: Gattex (USA), Revestive (EU/UK)
Category: Gastrointestinal Drugs
Teduglutide is a synthetic analogue of human glucagon-like peptide-2 (GLP-2) designed to enhance intestinal absorption by promoting mucosal growth, blood flow, and reduction of gastrointestinal secretions and motility in patients with short bowel syndrome.
Teduglutide — third party manufacturing & bulk supply
Teduglutide 5 mg vial is available through PharmaTradz for wholesale and bulk supply as well as on a third party (contract) manufacturing basis. Buyers sourcing this product generally take one of three routes:
Indicative minimum order quantity
Teduglutide is supplied as Injection — an injectable dosage form, so the indicative MOQ is 50,000 units. Actual MOQ is confirmed by the allocated manufacturer against your pack presentation and destination market. See full supply terms for dossier formats, market availability and shelf life.
Manufacturers of Teduglutide listed on PharmaTradz hold site-level approvals across WHO-GMP, EU-GMP, USFDA, ANVISA and TGA, verified at onboarding.
Request a quote for Teduglutide →Frequently Asked Questions
Teduglutide is used for the treatment of Short Bowel Syndrome (SBS) in patients who require parenteral nutrition. It helps improve intestinal absorption by enhancing mucosal growth and function, reducing dependence on intravenous feeding.
Teduglutide is a recombinant analog of human glucagon-like peptide-2 (GLP-2). It is a synthetic peptide that promotes intestinal growth and increases nutrient and fluid absorption in the gastrointestinal tract.
The trade name of Teduglutide is Gattex in the United States and Revestive in the European Union and the United Kingdom.
Teduglutide (Gattex/Revestive) is manufactured by Takeda Pharmaceuticals.
The generic name is Teduglutide.
The brand names are Gattex and Revestive.
Teduglutide is manufactured by Takeda Pharmaceuticals in facilities located in the United States, Switzerland, and other EU regions under strict regulatory standards for peptide-based therapeutics.
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