# Varenicline

NDC: 60687-648
Generic name: varenicline tartrate
Labeler / Manufacturer: American Health Packaging
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20220211
Marketing ended: 20261031
FDA application: ANDA201785

## 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:"60687-648"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=60687-648
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=16a03b5e-03e0-4b0b-92a4-aaf0669906f7