FdaApplication
ANDA 040667
Identifiers
- fda_app_no: ANDA040667
Properties
| Property | Value |
|---|---|
| applicant_name | HIKMA INTERNATIONAL PHARMACEUTICALS LLC |
| application_type | ANDA |
| approval_date | 2006-07-27 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| PRIMIDONE | PRIMIDONE | 50MG | TABLET;ORAL |
| PRIMIDONE | PRIMIDONE | 250MG | TABLET;ORAL |
2 products