# varenicline

NDC: 67877-744
Generic name: varenicline tartrate
Labeler / Manufacturer: Ascend Laboratories, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20230825

FDA application: ANDA214557

## Active ingredients

- VARENICLINE TARTRATE: 1 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"67877-744"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=67877-744
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e22e2a6a-66b4-459c-b978-51700e31a1a9