# nicotine

NDC: 37808-683
Generic name: nicotine polacrilex
Labeler / Manufacturer: H E B
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: GUM, CHEWING
Routes: ORAL
Marketing started: 20190701

FDA application: ANDA206393

## 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:"37808-683"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=37808-683
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=9bf10dfc-c6df-4cc9-ba79-2dcf874a2904