FDA NDC Directory · JSON-LD · Markdown

Varenicline

NDC 60687-648 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic namevarenicline tartrate
Labeler / ManufacturerAmerican Health Packaging
Marketing categoryAbbreviated NDA (generic) · App ANDA201785
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsVARENICLINE TARTRATE (1 mg/1)
Marketing started20220211
Marketing ended20261031
Package count1

External sources

Source: openFDA. Public-domain (CC0).