# Nicotine Polacrilex

NDC: 68016-293
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: 20171001
Marketing ended: 20270228
FDA application: ANDA204833

## Active ingredients

- NICOTINE: 4 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68016-293"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68016-293
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=9c115cd5-1952-4f1e-8e88-27f2c528e91f