Haloperidol
- Product NDC
- 50268-393
- 11-digit product format
- 502680393
- Labeler code
- 50268
- Product ID
- 50268-393_d5dd60ca-0c38-0dea-e053-2a95a90a1200
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Haloperidol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- AvPAK
- Application
- ANDA077580
- Marketing category
- ANDA
- Marketing start
- 2018-02-05
- Marketing end
- 0000-00-00
- Substance
- HALOPERIDOL
- Active strength
- 20 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 |
|---|
| 50268-393-15 | 50268039315 | 50 BLISTER PACK in 1 BOX, UNIT-DOSE (50268-393-15) > 1 TABLET in 1 BLISTER PACK (50268-393-11) | 50 blister pack | 2018-02-05 | 0000-00-00 | No | No | Current |