FdaApplication
ANDA 071221
Identifiers
- fda_app_no: ANDA071221
Properties
| Property | Value |
|---|---|
| applicant_name | DURAMED PHARMACEUTICALS INC SUB BARR LABORATORIES INC |
| application_type | ANDA |
| approval_date | 1987-07-07 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| HALOPERIDOL | HALOPERIDOL | 20MG | TABLET;ORAL |
1 product