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solifenacin succinate

NDC 31722-028 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerCamber Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA215761
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsSOLIFENACIN SUCCINATE (10 mg/1)
Marketing started20220615
Package count3

External sources

Source: openFDA. Public-domain (CC0).