# Nicotine

NDC: 63739-369
Generic name: Nicotine Polacrilex
Labeler / Manufacturer: McKesson Corporation dba SKY Packaging
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: GUM, CHEWING
Routes: ORAL
Marketing started: 20200427
Marketing ended: 20261130
FDA application: ANDA079219

## 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:"63739-369"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=63739-369
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=0b6880c8-04e7-418a-98d1-0c7d19e025b3