FdaApplication
ANDA 202385
Identifiers
- fda_app_no: ANDA202385
Properties
| Property | Value |
|---|---|
| applicant_name | AMNEAL PHARMACEUTICALS |
| application_type | ANDA |
| approval_date | 2011-12-16 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| FELBAMATE | FELBAMATE | 600MG/5ML | SUSPENSION;ORAL |
1 product