Haloperidol
- Product NDC
- 71335-2937
- 11-digit product format
- 713352937
- Labeler code
- 71335
- Product ID
- 71335-2937_01dbf8b5-6b02-43f2-bc9c-eee7c8da6cb1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Haloperidol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA218789
- Marketing category
- ANDA
- Marketing start
- 2024-04-19
- Substance
- HALOPERIDOL
- Active strength
- 2 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 |
|---|
| 71335-2937-1 | 71335293701 | 30 TABLET in 1 BOTTLE (71335-2937-1) | 30 tablet | 2025-10-28 | No | No | Historical |