FDA NDC Directory · JSON-LD · Markdown

VARENICLINE

NDC 72162-2218 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerBryant Ranch Prepack
Marketing categoryAbbreviated NDA (generic) · App ANDA201962
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsVARENICLINE TARTRATE (.5 mg/1)
Marketing started20230130
Package count1

External sources

Source: openFDA. Public-domain (CC0).