FDA NDC Directory · JSON-LD · Markdown

VARENICLINE TARTRATE

NDC 69315-402 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerLeading Pharma, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA217151
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsVARENICLINE TARTRATE (.5 mg/561)
Marketing started20231001
Package count1

External sources

Source: openFDA. Public-domain (CC0).