FdaApplication
ANDA 076773
Identifiers
- fda_app_no: ANDA076773
Properties
| Property | Value |
|---|---|
| applicant_name | SUN PHARMA CANADA INC |
| application_type | ANDA |
| approval_date | 2005-03-02 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| MICONAZOLE 3 | MICONAZOLE NITRATE | 4% | CREAM;VAGINAL |
1 product