FdaApplication
ANDA 213069
Identifiers
- fda_app_no: ANDA213069
Properties
| Property | Value |
|---|---|
| applicant_name | SUNSHINE LAKE PHARMA CO LTD |
| application_type | ANDA |
| approval_date | 2020-06-02 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| FEBUXOSTAT | FEBUXOSTAT | 40MG | TABLET;ORAL |
| FEBUXOSTAT | FEBUXOSTAT | 80MG | TABLET;ORAL |
2 products