FdaApplication
ANDA 071617
Identifiers
- fda_app_no: ANDA071617
Properties
| Property | Value |
|---|---|
| applicant_name | TEVA PHARMACEUTICALS USA |
| application_type | ANDA |
| approval_date | 1988-12-01 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| HALOPERIDOL | HALOPERIDOL LACTATE | EQ 2MG BASE/ML | CONCENTRATE;ORAL |
1 product