FdaApplication
ANDA 074444
Identifiers
- fda_app_no: ANDA074444
Properties
| Property | Value |
|---|---|
| applicant_name | SUN PHARMA CANADA INC |
| application_type | ANDA |
| approval_date | 1997-01-13 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| MICONAZOLE NITRATE | MICONAZOLE NITRATE | 2% | CREAM;VAGINAL |
1 product