# Nicotine

NDC: 59726-929
Generic name: nicotine polacrilex
Labeler / Manufacturer: P & L Development, LLC
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: GUM, CHEWING
Routes: ORAL
Marketing started: 20240301

FDA application: ANDA074507

## 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:"59726-929"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=59726-929
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c65c1c40-4c8f-40bb-ace4-8bbc9ecf630e