FdaApplication
NDA 019356
Identifiers
- fda_app_no: NDA019356
Properties
| Property | Value |
|---|---|
| applicant_name | LEGACY PHARMA INC SEZC |
| application_type | NDA |
| approval_date | 1990-06-18 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| NAFTIN | NAFTIFINE HYDROCHLORIDE | 1% | GEL;TOPICAL |
1 product