FdaApplication
NDA 015922
Identifiers
- fda_app_no: NDA015922
Properties
| Property | Value |
|---|---|
| applicant_name | ORTHO MCNEIL PHARMACEUTICAL |
| application_type | NDA |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| HALDOL | HALOPERIDOL LACTATE | EQ 2MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | CONCENTRATE;ORAL |
1 product