FdaApplication
ANDA 213852
Identifiers
- fda_app_no: ANDA213852
Properties
| Property | Value |
|---|---|
| applicant_name | RHODES PHARMACEUTICALS LP |
| application_type | ANDA |
| approval_date | 2021-09-07 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| AMPHETAMINE SULFATE | AMPHETAMINE SULFATE | 10MG | TABLET;ORAL |
| AMPHETAMINE SULFATE | AMPHETAMINE SULFATE | 5MG | TABLET;ORAL |
2 products