FDA NDC Directory · JSON-LD · Markdown

solifenacin succinate

NDC 68462-387 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED, EXTENDED RELEASE

Labeler / ManufacturerGlenmark Pharmaceuticals Inc., USA
Marketing categoryAbbreviated NDA (generic) · App ANDA209239
Dosage form / routeTABLET, FILM COATED, EXTENDED RELEASE · ORAL
Active ingredientsSOLIFENACIN SUCCINATE (10 mg/1)
Marketing started20190520
Package count3

External sources

Source: openFDA. Public-domain (CC0).