FdaApplication
ANDA 071217
Identifiers
- fda_app_no: ANDA071217
Properties
| Property | Value |
|---|---|
| applicant_name | DURAMED PHARMACEUTICALS INC SUB BARR LABORATORIES INC |
| application_type | ANDA |
| approval_date | 1986-12-04 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| HALOPERIDOL | HALOPERIDOL | 1MG | TABLET;ORAL |
1 product