FdaApplication
NDA 017244
Identifiers
- fda_app_no: NDA017244
Properties
| Property | Value |
|---|---|
| applicant_name | PARKE DAVIS DIV WARNER LAMBERT CO |
| application_type | NDA |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| UTICORT | BETAMETHASONE BENZOATE | 0.025% | GEL;TOPICAL |
1 product