FdaApplication
ANDA 075042
Identifiers
- fda_app_no: ANDA075042
Properties
| Property | Value |
|---|---|
| applicant_name | SUN PHARMA CANADA INC |
| application_type | ANDA |
| approval_date | 1998-08-25 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| HYDROCORTISONE VALERATE | HYDROCORTISONE VALERATE | 0.2% | CREAM;TOPICAL |
1 product