# Nicotine Polacrilex Coated Mint

NDC: 68016-285
Generic name: Nicotine Polacrilex
Labeler / Manufacturer: Chain Drug Consortium, LLC
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: GUM, CHEWING
Routes: BUCCAL
Marketing started: 20130901
Marketing ended: 20261231
FDA application: ANDA078697

## Active ingredients

- NICOTINE: 4 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68016-285"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68016-285
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b4ac0a22-3556-4591-aa7b-e09c6010adc8