FdaApplication
NDA 021844
Identifiers
- fda_app_no: NDA021844
Properties
| Property | Value |
|---|---|
| applicant_name | LEO PHARMA AS |
| application_type | NDA |
| approval_date | 2006-10-20 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| DESONATE | DESONIDE | 0.05% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | GEL;TOPICAL |
1 product