# NICORETTE

NDC: 0135-0635
Generic name: nicotine polacrilex
Labeler / Manufacturer: Haleon US Holdings LLC
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: LOZENGE
Routes: ORAL
Marketing started: 20220601

FDA application: ANDA077007

## 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:"0135-0635"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0135-0635
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=ffeb8286-860d-49f5-8df3-724afb4aaad8