FdaApplication
NDA 015921
Identifiers
- fda_app_no: NDA015921
Properties
| Property | Value |
|---|---|
| applicant_name | ORTHO MCNEIL PHARMACEUTICAL |
| application_type | NDA |
| approval_date | 1982-02-02 |
Products (6)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| HALDOL | HALOPERIDOL | 5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET;ORAL |
| HALDOL | HALOPERIDOL | 0.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET;ORAL |
| HALDOL | HALOPERIDOL | 2MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET;ORAL |
| HALDOL | HALOPERIDOL | 20MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET;ORAL |
| HALDOL | HALOPERIDOL | 10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET;ORAL |
| HALDOL | HALOPERIDOL | 1MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET;ORAL |
6 products