FdaApplication
NDA 021829
Identifiers
- fda_app_no: NDA021829
Properties
| Property | Value |
|---|---|
| applicant_name | UCB INC |
| application_type | NDA |
| approval_date | 2007-05-09 |
Products (6)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| NEUPRO | ROTIGOTINE | 6MG/24HR | FILM, EXTENDED RELEASE;TRANSDERMAL |
| NEUPRO | ROTIGOTINE | 2MG/24HR | FILM, EXTENDED RELEASE;TRANSDERMAL |
| NEUPRO | ROTIGOTINE | 3MG/24HR | FILM, EXTENDED RELEASE;TRANSDERMAL |
| NEUPRO | ROTIGOTINE | 1MG/24HR | FILM, EXTENDED RELEASE;TRANSDERMAL |
| NEUPRO | ROTIGOTINE | 4MG/24HR | FILM, EXTENDED RELEASE;TRANSDERMAL |
| NEUPRO | ROTIGOTINE | 8MG/24HR | FILM, EXTENDED RELEASE;TRANSDERMAL |
6 products