Haloperidol

Product NDC
0781-1393
11-digit product format
007811393
Labeler code
0781
Product ID
0781-1393_efbe4986-95cd-4ddb-8120-c6feacd2017f
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Haloperidol
Dosage form
TABLET
Route
ORAL
Labeler
Sandoz Inc
Application
ANDA071208
Marketing category
ANDA
Marketing start
1986-11-17
Marketing end
2020-12-31
Substance
HALOPERIDOL
Active strength
2 mg/1
Pharmacologic classes
Typical Antipsychotic [EPC]
NDC exclude flag
No
Listing certified through
0000-00-00
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

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0781-1393-01EA - Each0781-13932c902404-d683-4311-9582-f4f8e1d2b2f912012-07-24
0781-1393-10EA - Each0781-1393cb57575d-f3ff-4020-813c-aaf1a77188ef12012-07-24
0781-1393-13EA - Each0781-1393c7bff71e-b104-4c0c-8fff-b2c2a53583a012012-07-24

DailyMed Socrata Ingredients#

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
310671haloperidol 1 MG Oral TabletPSNdf0f93db-aa16-4f30-8c49-904d269b36b12
314034haloperidol 2 MG Oral TabletPSNdf0f93db-aa16-4f30-8c49-904d269b36b12
310672haloperidol 5 MG Oral TabletPSNdf0f93db-aa16-4f30-8c49-904d269b36b12
310671haloperidol 1 MG Oral TabletSCDdf0f93db-aa16-4f30-8c49-904d269b36b12
314034haloperidol 2 MG Oral TabletSCDdf0f93db-aa16-4f30-8c49-904d269b36b12
310672haloperidol 5 MG Oral TabletSCDdf0f93db-aa16-4f30-8c49-904d269b36b12