HALOPERIDOL (HALOPERIDOL LACTATE) — FDA Approval ANDA071187 (ABRAXIS PHARM)
HALOPERIDOL (HALOPERIDOL LACTATE) — FDA Approval ANDA071187 (ABRAXIS PHARM) is one of 9,000 drug approvals in the DrugApprovals dataset. Key details — Brand name: HALOPERIDOL; Active ingredients: HALOPERIDOL LACTATE; Application number: ANDA071187.
| Brand name | HALOPERIDOL |
|---|---|
| Active ingredients | HALOPERIDOL LACTATE |
| Application number | ANDA071187 |
| Sponsor | ABRAXIS PHARM |
| Dosage form | INJECTABLE |
| Route | INJECTION |
| Marketing status | Discontinued |
| Products in application | 1 |
| First approval date | 19870120 |
| Source | openFDA Drugs@FDA |
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