VARENICLINE
- Product NDC
- 60505-4795
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- VARENICLINE
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Apotex Corp
- Application
- ANDA201962
- Marketing category
- ANDA
- Substance
- VARENICLINE TARTRATE
- Current FDA listing
- Yes