FdaApplication
ANDA 201680
Identifiers
- fda_app_no: ANDA201680
Properties
| Property | Value |
|---|---|
| applicant_name | AMNEAL PHARMACEUTICALS |
| application_type | ANDA |
| approval_date | 2011-09-13 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| FELBAMATE | FELBAMATE | 400MG | TABLET;ORAL |
| FELBAMATE | FELBAMATE | 600MG | TABLET;ORAL |
2 products