Haloperidol
- Product NDC
- 71335-2912
- 11-digit product format
- 713352912
- Labeler code
- 71335
- Product ID
- 71335-2912_4254dc88-4869-ac08-e063-6294a90a5534
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Haloperidol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA071173
- Marketing category
- ANDA
- Marketing start
- 2019-11-25
- Substance
- HALOPERIDOL
- Active strength
- 5 mg/1
- Pharmacologic classes
- Typical Antipsychotic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| J6292F8L3D | HALOPERIDOL | 52-86-8 | HALOPERIDOL |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 71335-2912-1 | 71335291201 | 100 TABLET in 1 BOTTLE (71335-2912-1) | 100 tablet | 2025-10-29 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Haloperidol Tablets, USP | Bryant Ranch Prepack | 2025-10-29 | HUMAN PRESCRIPTION DRUG LABEL | 100 |