HALDOL (HALOPERIDOL LACTATE) — FDA Approval NDA015922 (ORTHO MCNEIL)
HALDOL (HALOPERIDOL LACTATE) — FDA Approval NDA015922 (ORTHO MCNEIL) is one of 9,000 drug approvals in the DrugApprovals dataset. Key details — Brand name: HALDOL; Active ingredients: HALOPERIDOL LACTATE; Application number: NDA015922.
| Brand name | HALDOL |
|---|---|
| Active ingredients | HALOPERIDOL LACTATE |
| Application number | NDA015922 |
| Sponsor | ORTHO MCNEIL |
| Dosage form | CONCENTRATE |
| Route | ORAL |
| Marketing status | Discontinued |
| Products in application | 1 |
| First approval date | 19670412 |
| Source | openFDA Drugs@FDA |
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