# QUITINE NICOTINE

NDC: 84720-012
Generic name: Nicotine polacrilex
Labeler / Manufacturer: QUITINE LLC
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: GUM, CHEWING
Routes: ORAL
Marketing started: 20260806

FDA application: ANDA206394

## Active ingredients

- NICOTINE: 2 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"84720-012"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=84720-012
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=1f93571c-4bd2-4272-ab9f-240b7c8a024b