# VARENICLINE

NDC: 60290-077
Generic name: VARENICLINE
Labeler / Manufacturer: Umedica Laboratories USA Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20260109

FDA application: ANDA218985

## Active ingredients

- VARENICLINE TARTRATE: .5 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"60290-077"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=60290-077
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f2e57493-d099-4055-8e92-67611c8d20f4