FdaApplication
ANDA 071076
Identifiers
- fda_app_no: ANDA071076
Properties
| Property | Value |
|---|---|
| applicant_name | PUREPAC PHARMACEUTICAL CO |
| application_type | ANDA |
| approval_date | 1987-08-04 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| HALOPERIDOL | HALOPERIDOL | 20MG | TABLET;ORAL |
1 product