FdaApplication
NDA 217900
Identifiers
- fda_app_no: NDA217900
Properties
| Property | Value |
|---|---|
| applicant_name | SUN PHARMACEUTICAL INDUSTRIES INC |
| application_type | NDA |
| approval_date | 2024-07-25 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| LEQSELVI | DEURUXOLITINIB PHOSPHATE | EQ 8MG BASE | TABLET;ORAL |
1 product