# Nicotine Polacrilex

NDC: 0363-9240
Generic name: Nicotine Polacrilex
Labeler / Manufacturer: Walgreens
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: GUM, CHEWING
Routes: ORAL
Marketing started: 20201030
Marketing ended: 20270330
FDA application: ANDA079216

## 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:"0363-9240"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0363-9240
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b1174e20-e1ad-4c58-8b32-683b7e98fca9