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Solifenacin succinate

NDC 72303-0831 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic namesolifenacin succinate
Labeler / ManufacturerHEC Pharm USA Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA213346
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsSOLIFENACIN SUCCINATE (5 mg/1)
Marketing started20260701
Package count2

External sources

Source: openFDA. Public-domain (CC0).