FdaApplication
ANDA 211049
Identifiers
- fda_app_no: ANDA211049
Properties
| Property | Value |
|---|---|
| applicant_name | SUNSHINE LAKE PHARMA CO LTD |
| application_type | ANDA |
| approval_date | 2019-02-22 |
Products (3)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| OLMESARTAN MEDOXOMIL | OLMESARTAN MEDOXOMIL | 5MG | TABLET;ORAL |
| OLMESARTAN MEDOXOMIL | OLMESARTAN MEDOXOMIL | 20MG | TABLET;ORAL |
| OLMESARTAN MEDOXOMIL | OLMESARTAN MEDOXOMIL | 40MG | TABLET;ORAL |
3 products