# NICODERM CQ

NDC: 0135-0195
Generic name: nicotine
Labeler / Manufacturer: Haleon US Holdings LLC
Product type: HUMAN OTC DRUG
Marketing category: New Drug Application (innovator)
Dosage form: PATCH, EXTENDED RELEASE
Routes: TRANSDERMAL
Marketing started: 20110512

FDA application: NDA020165

## Active ingredients

- NICOTINE: 14 mg/24h

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0135-0195"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0135-0195
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=93b2d1b9-83c1-40b5-b6af-90c38c8d6cef