FdaApplication
ANDA 206901
Identifiers
- fda_app_no: ANDA206901
Properties
| Property | Value |
|---|---|
| applicant_name | SUN PHARMA CANADA INC |
| application_type | ANDA |
| approval_date | 2016-01-06 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| NAFTIFINE HYDROCHLORIDE | NAFTIFINE HYDROCHLORIDE | 2% | CREAM;TOPICAL |
1 product