# Nicotine Polacrilex original

NDC: 0363-1608
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: 20140101

FDA application: ANDA074507

## Active ingredients

- NICOTINE: 2 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0363-1608"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0363-1608
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f759d9b2-35e0-4b88-9219-4c0e483af5c4
