FdaApplication
ANDA 219800
Identifiers
- fda_app_no: ANDA219800
Properties
| Property | Value |
|---|---|
| applicant_name | GRANULES PHARMACEUTICALS INC |
| application_type | ANDA |
Products (6)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| AMPHETAMINE | AMPHETAMINE | 15.7MG | TABLET, ORALLY DISINTEGRATING;ORAL |
| AMPHETAMINE | AMPHETAMINE | 3.1MG | TABLET, ORALLY DISINTEGRATING;ORAL |
| AMPHETAMINE | AMPHETAMINE | 18.8MG | TABLET, ORALLY DISINTEGRATING;ORAL |
| AMPHETAMINE | AMPHETAMINE | 6.3MG | TABLET, ORALLY DISINTEGRATING;ORAL |
| AMPHETAMINE | AMPHETAMINE | 9.4MG | TABLET, ORALLY DISINTEGRATING;ORAL |
| AMPHETAMINE | AMPHETAMINE | 12.5MG | TABLET, ORALLY DISINTEGRATING;ORAL |
6 products