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Oxybutynin Chloride

NDC 52817-261 · HUMAN PRESCRIPTION DRUG · TABLET

Generic nameoxybutynin chloride
Labeler / ManufacturerTruPharma LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA210125
Dosage form / routeTABLET · ORAL
Active ingredientsOXYBUTYNIN CHLORIDE (2.5 mg/1)
Marketing started20260728
Package count1

External sources

Source: openFDA. Public-domain (CC0).