FdaApplication
ANDA 076730
Identifiers
- fda_app_no: ANDA076730
Properties
| Property | Value |
|---|---|
| applicant_name | SUN PHARMA CANADA INC |
| application_type | ANDA |
| approval_date | 2004-07-29 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| ALCLOMETASONE DIPROPIONATE | ALCLOMETASONE DIPROPIONATE | 0.05% | OINTMENT;TOPICAL |
1 product