# Nicotine transdermal system step 1

NDC: 63868-735
Generic name: Nicotine
Labeler / Manufacturer: Chain Drug Marketing Association INC
Product type: HUMAN OTC DRUG
Marketing category: New Drug Application (innovator)
Dosage form: PATCH, EXTENDED RELEASE
Routes: TRANSDERMAL
Marketing started: 20201031

FDA application: NDA020076

## Active ingredients

- NICOTINE: 21 mg/24h

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"63868-735"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=63868-735
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=df1348cb-0d15-7e4b-921c-d8764c858e66