FdaApplication
ANDA 206165
Identifiers
- fda_app_no: ANDA206165
Properties
| Property | Value |
|---|---|
| applicant_name | AMNEAL PHARMACEUTICALS LLC |
| application_type | ANDA |
| approval_date | 2019-03-20 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| NAFTIFINE HYDROCHLORIDE | NAFTIFINE HYDROCHLORIDE | 1% | GEL;TOPICAL |
1 product