FdaApplication
ANDA 076216
Identifiers
- fda_app_no: ANDA076216
Properties
| Property | Value |
|---|---|
| applicant_name | SUN PHARMA CANADA INC |
| application_type | ANDA |
| approval_date | 2004-05-28 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| AMMONIUM LACTATE | AMMONIUM LACTATE | EQ 12% BASE | LOTION;TOPICAL |
1 product