FdaApplication
NDA 207154
Identifiers
- fda_app_no: NDA207154
Properties
| Property | Value |
|---|---|
| applicant_name | ALMIRALL LLC |
| application_type | NDA |
| approval_date | 2016-02-24 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| ACZONE | DAPSONE | 7.5% | GEL;TOPICAL |
1 product