FdaApplication
ANDA 211335
Identifiers
- fda_app_no: ANDA211335
Properties
| Property | Value |
|---|---|
| applicant_name | SUNSHINE LAKE PHARMA CO LTD |
| application_type | ANDA |
| approval_date | 2019-03-26 |
Products (4)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| TADALAFIL | TADALAFIL | 20MG | TABLET;ORAL |
| TADALAFIL | TADALAFIL | 10MG | TABLET;ORAL |
| TADALAFIL | TADALAFIL | 2.5MG | TABLET;ORAL |
| TADALAFIL | TADALAFIL | 5MG | TABLET;ORAL |
4 products