Haloperidol
- Product NDC
- 0904-7242
- 11-digit product format
- 009047242
- Labeler code
- 0904
- Product ID
- 0904-7242_39607d71-0463-4c9b-bf6f-b39eaa006e85
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Haloperidol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Major Pharmaceuticals
- Application
- ANDA071173
- Marketing category
- ANDA
- Marketing start
- 2021-02-18
- Marketing end
- 0000-00-00
- Substance
- HALOPERIDOL
- Active strength
- 2 mg/1
- Pharmacologic classes
- Typical Antipsychotic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0904-7242-61 | 00904724261 | 100 BLISTER PACK in 1 CARTON (0904-7242-61) > 1 TABLET in 1 BLISTER PACK | 100 blister pack | 2022-08-09 | 0000-00-00 | No | No | Current |