Haloperidol
- Product NDC
- 50090-4365
- 11-digit product format
- 500904365
- Labeler code
- 50090
- Product ID
- 50090-4365_c7e6a7bf-505d-4886-b1f2-0bf2f3bede80
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Haloperidol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA077580
- Marketing category
- ANDA
- Marketing start
- 2008-01-03
- Marketing end
- 0000-00-00
- Substance
- HALOPERIDOL
- Active strength
- 5 mg/1
- Pharmacologic classes
- Typical Antipsychotic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-4365-0 | 50090436500 | 33 BLISTER PACK in 1 BOX, UNIT-DOSE (50090-4365-0) > 1 TABLET in 1 BLISTER PACK | 33 blister pack | 2019-06-18 | 0000-00-00 | No | No | Current |