Active ingredient
Rotigotine
6 finished FDA listings contain Rotigotine as their only active ingredient.
FDA NDC Directory
- Ingredient names as written by FDA
- ROTIGOTINE, ROTIGOTINE HYDROCHLORIDE
- Dosage forms
- Patch, Extended Release
- Routes
- Transdermal
- Manufacturers / labelers
- 1
- Strengths listed
- 1 mg/24h · 2 mg/24h · 3 mg/24h · 4 mg/24h · 6 mg/24h · 8 mg/24h
- Brand names in FDA listings
- Neupro
RxNorm (National Library of Medicine)
Ingredient concept RxCUI 616739
Drugs@FDA applications
Linked only where the FDA listing’s application number matches Drugs@FDA exactly. A listing in the NDC Directory does not by itself mean FDA approval.
| Application | Sponsor | Original approval | Listings |
|---|---|---|---|
| NDA 021829 | UCB INC | 2007-05-09 | 6 |
Official labeling on DailyMed
No DailyMed labels matched by set ID.
Sources: FDA NDC Directory (2026-09-29), RxNorm, Drugs@FDA, DailyMed. Each source’s facts are shown separately as published.