# VARENICLINE TARTRATE

NDC: 69315-403
Generic name: VARENICLINE TARTRATE
Labeler / Manufacturer: Leading Pharma, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20231001

FDA application: ANDA217151

## Active ingredients

- VARENICLINE TARTRATE: 1 mg/561

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"69315-403"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=69315-403
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=fdb36cfa-d20a-4fd9-b994-a5d16e4bb438