# OXYTROL

NDC: 0023-6153
Generic name: Oxybutynin
Labeler / Manufacturer: Allergan, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: PATCH
Routes: TRANSDERMAL
Marketing started: 20030226

FDA application: NDA021351

## Active ingredients

- OXYBUTYNIN: 3.9 mg/d

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0023-6153"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0023-6153
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=20dee37f-1412-44ed-9e8b-f4379ce23eb0