FdaApplication
ANDA 205181
Identifiers
- fda_app_no: ANDA205181
Properties
| Property | Value |
|---|---|
| applicant_name | SUN PHARMA CANADA INC |
| application_type | ANDA |
| approval_date | 2017-11-16 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| BUTENAFINE HYDROCHLORIDE | BUTENAFINE HYDROCHLORIDE | 1% | CREAM;TOPICAL |
1 product