FdaApplication
ANDA 216918
Identifiers
- fda_app_no: ANDA216918
Properties
| Property | Value |
|---|---|
| applicant_name | MANKIND PHARMA LTD |
| application_type | ANDA |
| approval_date | 2024-04-11 |
Products (6)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| HALOPERIDOL | HALOPERIDOL | 10MG | TABLET;ORAL |
| HALOPERIDOL | HALOPERIDOL | 0.5MG | TABLET;ORAL |
| HALOPERIDOL | HALOPERIDOL | 20MG | TABLET;ORAL |
| HALOPERIDOL | HALOPERIDOL | 1MG | TABLET;ORAL |
| HALOPERIDOL | HALOPERIDOL | 2MG | TABLET;ORAL |
| HALOPERIDOL | HALOPERIDOL | 5MG | TABLET;ORAL |
6 products