# NICOTINE TRANSDERMAL

NDC: 11822-3627
Generic name: NICOTINE
Labeler / Manufacturer: Rite Aid Corporation
Product type: HUMAN OTC DRUG
Marketing category: New Drug Application (innovator)
Dosage form: KIT
Routes: TRANSDERMAL
Marketing started: 20210331

FDA application: NDA020076

## Active ingredients

—

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"11822-3627"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=11822-3627
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=ae6027da-5c96-ed47-e1ae-e900fc0f72ce