FdaApplication
NDA 022129
Identifiers
- fda_app_no: NDA022129
Properties
| Property | Value |
|---|---|
| applicant_name | SHIONOGI INC |
| application_type | NDA |
| approval_date | 2009-04-09 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| ULESFIA | BENZYL ALCOHOL | 5% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | LOTION;TOPICAL |
1 product