Composition
- Active ingredients
- HALOPERIDOL 20MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Strengths and forms
The FDA lists each strength of a product separately; these pages share one label.
- HALOPERIDOL 0.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** · TabletNDA015921-001 · Discontinued
- HALOPERIDOL 20MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** · TabletThis page
- HALOPERIDOL 5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** · TabletNDA015921-004 · Discontinued
- HALOPERIDOL 1MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** · TabletNDA015921-002 · Discontinued
- HALOPERIDOL 10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** · TabletNDA015921-005 · Discontinued
- HALOPERIDOL 2MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** · TabletNDA015921-003 · Discontinued
Official product information
Drugs@FDA lists the approved labels, letters and reviews for application NDA015921.
At a glance
- Brand name
- Haldol
- Active substance
- haloperidol
- Route
- Oral
- Dosage form
- Tablet
- Applicant
- Ortho Mcneil
- Status
- Discontinued
- FDA approval
- 12 Apr 1967
- Application
- NDA015921-006