Haloperidol

Product NDC
50436-0233
11-digit product format
504360233
Labeler code
50436
Product ID
50436-0233_fa7eb5bf-7a20-4183-ba41-e8d5c6c4b3a8
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Haloperidol
Dosage form
TABLET
Route
ORAL
Labeler
Unit Dose Services
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
2020-12-31
Current FDA listing
Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
d599bae4-cb25-0798-7468-31aa188fb750Product name720260304
6aae29ef-bf3c-3ebb-3bf1-10ee5424a22eProduct name220250114
af58e43a-5792-c2c1-8e57-a2454df1f2c0Product name320240202
ce329990-eb12-45a5-87d5-ce5ef054ca71Product name220190930

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
50436-0233-42021-01-29C16284748780-1ba0f9c33-2d6f-a910-e053-dadaa90a0b85Haloperidol Tablets, USP

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
50436-0233-4Haloperidol14 in 1 BOTTLETABLET143

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
50436-0233HALOPERIDOL TABLET [UNIT DOSE SERVICES]3Legacy NDC, 1 package rows20181010_6ca34b20-df63-46a0-9d31-fe2bd3311a18.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
310672haloperidol 5 MG Oral TabletPSN6ca34b20-df63-46a0-9d31-fe2bd3311a183
310672haloperidol 5 MG Oral TabletSCD6ca34b20-df63-46a0-9d31-fe2bd3311a183

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionStatus
50436-0233-45043602330414 in 1 BOTTLEHistorical