# Nicotine Transdermal System

NDC: 46122-353
Generic name: Nicotine Transdermal System
Labeler / Manufacturer: AmerisourceBergen Drug Corporation
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: PATCH, EXTENDED RELEASE
Routes: TRANSDERMAL
Marketing started: 20240625

FDA application: ANDA074612

## 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:"46122-353"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=46122-353
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=8a5c7835-3ab1-b3f8-e9db-e5d0cb42b59e