FdaApplication
ANDA 207116
Identifiers
- fda_app_no: ANDA207116
Properties
| Property | Value |
|---|---|
| applicant_name | SUN PHARMA CANADA INC |
| application_type | ANDA |
| approval_date | 2020-04-27 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| MUPIROCIN | MUPIROCIN CALCIUM | EQ 2% BASE | CREAM;TOPICAL |
1 product