# Nicotine Polacrilex

NDC: 0363-3290
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: 20270205
FDA application: ANDA204833

## 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:"0363-3290"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0363-3290
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=5741531a-3886-4b0a-ae92-d7c238488fdf