FdaApplication
ANDA 077092
Identifiers
- fda_app_no: ANDA077092
Properties
| Property | Value |
|---|---|
| applicant_name | SUN PHARMA CANADA INC |
| application_type | ANDA |
| approval_date | 2005-08-10 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| CICLOPIROX | CICLOPIROX | 0.77% | SUSPENSION;TOPICAL |
1 product