← FDA Drug Approvals (Drugs@FDA)
NEUPRO
NDA · New Drug Application · Sponsor: UCB INC · Approved 2007-05-09
Drug application
- FDA Application #
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
- Authoritative
- Drugs@FDA application overview
- Machine
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