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Solifenacin Succinate

NDC 35561-286 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic namesolifenacin succinate
Labeler / ManufacturerBostal LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA210281
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsSOLIFENACIN SUCCINATE (10 mg/1)
Marketing started20190520
Package count4

External sources

Source: openFDA. Public-domain (CC0).