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Varenicline

NDC 10135-808 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic nameVarenicline tartrate
Labeler / ManufacturerMarlex Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA217283
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsVARENICLINE TARTRATE (.5 mg/1)
Marketing started20250101
Package count1

External sources

Source: openFDA. Public-domain (CC0).