FdaApplication
ANDA 083901
Identifiers
- fda_app_no: ANDA083901
Properties
| Property | Value |
|---|---|
| applicant_name | LANNETT CO INC |
| application_type | ANDA |
| approval_date | 1984-08-31 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| AMPHETAMINE SULFATE | AMPHETAMINE SULFATE | 10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET;ORAL |
| AMPHETAMINE SULFATE | AMPHETAMINE SULFATE | 5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET;ORAL |
2 products