FdaApplication
ANDA 206669
Identifiers
- fda_app_no: ANDA206669
Properties
| Property | Value |
|---|---|
| applicant_name | SUNSHINE LAKE PHARMA CO LTD |
| application_type | ANDA |
| approval_date | 2018-10-03 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| ENTACAPONE | ENTACAPONE | 200MG | TABLET;ORAL |
1 product