FdaApplication
ANDA 207175
Identifiers
- fda_app_no: ANDA207175
Properties
| Property | Value |
|---|---|
| applicant_name | HISUN PHARMACEUTICAL (HANGZHOU) CO LTD |
| application_type | ANDA |
| approval_date | 2017-09-28 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| LEVETIRACETAM | LEVETIRACETAM | 500MG | TABLET, EXTENDED RELEASE;ORAL |
| LEVETIRACETAM | LEVETIRACETAM | 750MG | TABLET, EXTENDED RELEASE;ORAL |
2 products