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Oxybutynin Chloride

NDC 71610-860 · HUMAN PRESCRIPTION DRUG · TABLET

Generic nameoxybutynin chloride
Labeler / ManufacturerAphena Pharma Solutions - Tennessee, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA075079
Dosage form / routeTABLET · ORAL
Active ingredientsOXYBUTYNIN CHLORIDE (5 mg/1)
Marketing started20220930
Package count4

External sources

Source: openFDA. Public-domain (CC0).