Vibegron 75 mg Suppliers & Bulk Manufacturers
Available Forms: Tablets
Available Strengths: 75 mg
Reference Brands: Gemtesa (USA), Obgemsa (EU/UK)
Category: Gastrointestinal Drugs
Vibegron is a selective β₃-adrenergic receptor agonist used to treat symptoms of overactive bladder (OAB) such as urinary urgency, frequency and urge urinary incontinence in adults (including men with BPH being treated). It works by relaxing the bladder’s detrusor muscle, increasing storage capacity and reducing incontinence episodes.
Vibegron — third party manufacturing & bulk supply
Vibegron 75 mg 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
Vibegron is supplied as Tablets — an oral solid dosage form, so the indicative MOQ is 200,000 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 Vibegron listed on PharmaTradz hold site-level approvals across WHO-GMP, EU-GMP, USFDA, ANVISA and TGA, verified at onboarding.
Request a quote for Vibegron →Frequently Asked Questions
Vibegron is used to treat overactive bladder (OAB) with symptoms such as urinary urgency, increased frequency, and urge urinary incontinence. It works by relaxing the bladder’s detrusor muscle, allowing it to hold more urine and reducing sudden urges to urinate.
Vibegron is made from the active ingredient vibegron, a selective beta-3 adrenergic receptor agonist that enhances bladder relaxation during the storage phase of the urinary cycle.
The trade name of Vibegron is Gemtesa.
Vibegron (Gemtesa) is developed and marketed by Urovant Sciences, a subsidiary of Sumitovant Biopharma and part of the Sumitomo Pharma Group.
The generic name is Vibegron.
The brand name is Gemtesa.
Vibegron is manufactured by Urovant Sciences in the United States and Japan under the quality and regulatory standards of the U.S. FDA and Japan’s PMDA.
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