FdaApplication
ANDA 076679
Identifiers
- fda_app_no: ANDA076679
Properties
| Property | Value |
|---|---|
| applicant_name | SUN PHARMA CANADA INC |
| application_type | ANDA |
| approval_date | 2004-12-21 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| MOMETASONE FUROATE | MOMETASONE FUROATE | 0.1% | CREAM;TOPICAL |
1 product