# NEUPRO
> **NDA021829** · New Drug Application · Sponsor: UCB INC · Approved 2007-05-09
## Drug
- **FDA Application Number:** NDA021829
- **Application type:** New Drug Application
- **Brand name:** NEUPRO
- **Generic name:** ROTIGOTINE
- **Active ingredients:** ROTIGOTINE
- **Dosage form:** FILM, EXTENDED RELEASE
- **Route:** TRANSDERMAL
- **Marketing status:** Prescription
- **Sponsor:** UCB INC
- **Manufacturer:** UCB, Inc.
- **First approval:** 2007-05-09
## Source
- [Drugs@FDA application overview](https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=021829)
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