FdaApplication
ANDA 213914
Identifiers
- fda_app_no: ANDA213914
Properties
| Property | Value |
|---|---|
| applicant_name | SUN PHARMACEUTICAL INDUSTRIES LTD |
| application_type | ANDA |
| approval_date | 2021-08-16 |
Products (4)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| SUNITINIB MALATE | SUNITINIB MALATE | EQ 37.5MG BASE | CAPSULE;ORAL |
| SUNITINIB MALATE | SUNITINIB MALATE | EQ 50MG BASE | CAPSULE;ORAL |
| SUNITINIB MALATE | SUNITINIB MALATE | EQ 12.5MG BASE | CAPSULE;ORAL |
| SUNITINIB MALATE | SUNITINIB MALATE | EQ 25MG BASE | CAPSULE;ORAL |
4 products