FdaApplication
ANDA 213037
Identifiers
- fda_app_no: ANDA213037
Properties
| Property | Value |
|---|---|
| applicant_name | SUNSHINE LAKE PHARMA CO LTD |
| application_type | ANDA |
| approval_date | 2023-10-02 |
Products (3)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| ARIPIPRAZOLE | ARIPIPRAZOLE | 2MG | TABLET;ORAL |
| ARIPIPRAZOLE | ARIPIPRAZOLE | 5MG | TABLET;ORAL |
| ARIPIPRAZOLE | ARIPIPRAZOLE | 10MG | TABLET;ORAL |
3 products