# HALDOL
> **NDA015921** · New Drug Application · Sponsor: ORTHO MCNEIL · Approved 1967-04-12
## Drug
- **FDA Application Number:** NDA015921
- **Application type:** New Drug Application
- **Brand name:** HALDOL
- **Generic name:** Haloperidol
- **Active ingredients:** HALOPERIDOL
- **Dosage form:** TABLET
- **Route:** ORAL
- **Marketing status:** Discontinued
- **Sponsor:** ORTHO MCNEIL
- **First approval:** 1967-04-12
## Source
- [Drugs@FDA application overview](https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=015921)
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