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varenicline

NDC 67877-744 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic namevarenicline tartrate
Labeler / ManufacturerAscend Laboratories, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA214557
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsVARENICLINE TARTRATE (1 mg/1)
Marketing started20230825
Package count2

External sources

Source: openFDA. Public-domain (CC0).