# nicotine

NDC: 37808-849
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: 20190416

FDA application: ANDA076789

## 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:"37808-849"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=37808-849
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=bbc4fd9f-b1f5-4691-b980-3424c91e4c88