# Neupro

NDC: 50474-808
Generic name: rotigotine
Labeler / Manufacturer: UCB, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: KIT
Routes: —
Marketing started: 20120402

FDA application: NDA021829

## Active ingredients

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## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"50474-808"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=50474-808
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=939e28c5-f3a9-42c0-9a2d-8d471d82a6e0