# Neupro

NDC: 50474-802
Generic name: rotigotine
Labeler / Manufacturer: UCB, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: PATCH, EXTENDED RELEASE
Routes: TRANSDERMAL
Marketing started: 20120402

FDA application: NDA021829

## Active ingredients

- ROTIGOTINE: 2 mg/24h

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"50474-802"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=50474-802
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=939e28c5-f3a9-42c0-9a2d-8d471d82a6e0