FdaApplication
ANDA 070062
Identifiers
- fda_app_no: ANDA070062
Properties
| Property | Value |
|---|---|
| applicant_name | SUN PHARMA CANADA INC |
| application_type | ANDA |
| approval_date | 1985-05-14 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| BETAMETHASONE VALERATE | BETAMETHASONE VALERATE | EQ 0.1% BASE | CREAM;TOPICAL |
1 product