FdaApplication
ANDA 211139
Identifiers
- fda_app_no: ANDA211139
Properties
| Property | Value |
|---|---|
| applicant_name | AMNEAL PHARMACEUTICALS OF NEW YORK LLC |
| application_type | ANDA |
| approval_date | 2018-09-26 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| AMPHETAMINE SULFATE | AMPHETAMINE SULFATE | 10MG | TABLET;ORAL |
| AMPHETAMINE SULFATE | AMPHETAMINE SULFATE | 5MG | TABLET;ORAL |
2 products