FdaApplication
ANDA 210191
Identifiers
- fda_app_no: ANDA210191
Properties
| Property | Value |
|---|---|
| applicant_name | SUN PHARMA CANADA INC |
| application_type | ANDA |
| approval_date | 2019-06-26 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| DAPSONE | DAPSONE | 7.5% | GEL;TOPICAL |
1 product