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Varenicline tartrate

NDC 71921-308 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerFlorida Pharmaceutical Products, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA219106
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsVARENICLINE TARTRATE (.5 mg/1)
Marketing started20241101
Package count1

External sources

Source: openFDA. Public-domain (CC0).