FdaApplication
ANDA 205076
Identifiers
- fda_app_no: ANDA205076
Properties
| Property | Value |
|---|---|
| applicant_name | SUN PHARMA CANADA INC |
| application_type | ANDA |
| approval_date | 2016-03-07 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| OXICONAZOLE NITRATE | OXICONAZOLE NITRATE | EQ 1% BASE | CREAM;TOPICAL |
1 product