# Nicotine Polacrilex, Original

NDC: 68016-286
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: 20130701
Marketing ended: 20261231
FDA application: ANDA074507

## Active ingredients

- NICOTINE: 2 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68016-286"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68016-286
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=cb67cd5e-9264-4530-a678-da299476f356