FdaApplication
ANDA 209822
Identifiers
- fda_app_no: ANDA209822
Properties
| Property | Value |
|---|---|
| applicant_name | TEVA PHARMACEUTICALS USA |
| application_type | ANDA |
| approval_date | 2019-01-14 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| VIGABATRIN | VIGABATRIN | 500MG | TABLET;ORAL |
1 product