# varenicline tartrate

NDC: 43598-022
Generic name: varenicline tartrate
Labeler / Manufacturer: Dr. Reddys Laboratories Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: KIT
Routes: ORAL
Marketing started: 20241213

FDA application: ANDA215931

## Active ingredients

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## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"43598-022"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=43598-022
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=16ee0a83-88d7-97de-1e07-f9e6dcb5c934