FdaApplication
ANDA 211061
Identifiers
- fda_app_no: ANDA211061
Properties
| Property | Value |
|---|---|
| applicant_name | APPCO PHARMA LLC |
| application_type | ANDA |
| approval_date | 2020-01-08 |
Products (6)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| HALOPERIDOL | HALOPERIDOL | 10MG | TABLET;ORAL |
| HALOPERIDOL | HALOPERIDOL | 0.5MG | TABLET;ORAL |
| HALOPERIDOL | HALOPERIDOL | 1MG | TABLET;ORAL |
| HALOPERIDOL | HALOPERIDOL | 20MG | TABLET;ORAL |
| HALOPERIDOL | HALOPERIDOL | 2MG | TABLET;ORAL |
| HALOPERIDOL | HALOPERIDOL | 5MG | TABLET;ORAL |
6 products