Haloperidol
- Product NDC
- 50090-4400
- 11-digit product format
- 500904400
- Labeler code
- 50090
- Product ID
- 50090-4400_f9692cbb-611b-43ab-ac4d-8a16cf0ebd43
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- haloperidol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA070278
- Marketing category
- ANDA
- Marketing start
- 1986-06-10
- Marketing end
- 0000-00-00
- Substance
- HALOPERIDOL
- Active strength
- 2 mg/1
- Pharmacologic classes
- Typical Antipsychotic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
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 | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-4400-0 | 50090440000 | 33 TABLET in 1 BOTTLE (50090-4400-0) | 33 tablet | 2019-06-28 | 0000-00-00 | No | No | Current |