FdaApplication
NDA 204286
Identifiers
- fda_app_no: NDA204286
Properties
| Property | Value |
|---|---|
| applicant_name | LEGACY PHARMA INC SEZC |
| application_type | NDA |
| approval_date | 2013-06-27 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| NAFTIN | NAFTIFINE HYDROCHLORIDE | 2% | GEL;TOPICAL |
1 product