FDA NDC Directory · JSON-LD · Markdown

Solifenacin Succinate

NDC 65862-879 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerAurobindo Pharma Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA206817
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsSOLIFENACIN SUCCINATE (10 mg/1)
Marketing started20221227
Package count4

External sources

Source: openFDA. Public-domain (CC0).