NDC 0832-1550-89 - Haloperidol

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC: 0832-1550
Requested NDC: 0832-1550-89
Package NDCs from labels: 0832-1550-11, 0832-1550-89, 0832-1550-01
Manufacturer: Upsher-Smith Laboratories, LLC | Appco Pharma, LLC
Effective date: 2026-08-05
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Haloperidol - Upsher-Smith Laboratories, LLC \| Appco Pharma, LLC	Upsher-Smith Laboratories, LLC \| Appco Pharma, LLC	2026-08-05	HUMAN PRESCRIPTION DRUG LABEL
Haloperidol Tablets, USP	REMEDYREPACK INC.	2025-04-03	HUMAN PRESCRIPTION DRUG LABEL
Haloperidol - NCS HealthCare of KY, LLC dba Vangard Labs	NCS HealthCare of KY, LLC dba Vangard Labs	2024-10-18	HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
0832-1550-01	Haloperidol	100 in 1 CARTON	TABLET	100	6
0832-1550-11	Haloperidol	100 in 1 BOTTLE	TABLET	100	6
0832-1550-89	Haloperidol	1 in 1 BLISTER PACK	TABLET	1	6

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
0832-1550	HALOPERIDOL TABLET [UPSHER-SMITH LABORATORIES, LLC]	6	Current NDC, Legacy NDC, 3 package rows	20250419_afb3ac3e-7459-42d3-b5ca-e0d6d27ced73.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
0832-1550-01	EA - Each	0832-1550	25e8a8bd-f8e0-4cf9-b2ea-d5eb6e3bf2f5	1	2022-11-07
0832-1550-11	EA - Each	0832-1550	df5b9013-6ff1-499c-a08e-6550bca63adf	1	2020-02-13
0832-1550-89	EA - Each	0832-1550	de7448a1-e624-4764-837a-9e65444f7ade	1	2022-11-07

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 35 of 35 · 683 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Tox-Chord	ALFALFA, ALUMINA, BENZOICUM ACIDUM, CARBONEUM, CETRARIA ISLANDICA, FOLLICULINUM, FUCUS VESICULOSUS, FUMARICUM ACIDUM, HEPAR SUIS, KALI CARBONICUM, KREOSOTUM, NATRUM MURIATICUM, PARAFFINUM, PETROLEUM, PHOSPHORICUM ACIDUM, PHOSPHORUS, PIX LIQUIDA, PLANTAGO MAJOR, PLUMBUM METALLICUM, PULSATILLA (VULGARIS), RADIUM BROMATUM, RESORCINUM, SALOL, SILICEA, SYMPHYTUM OFFICINALE, TABACUM, TEREBINTHINA, THYROIDINUM (BOVINE), TRITICUM REPENS, ZINCUM OXYDATUM	Energetix Corp	6b0d1628-b20d-426e-9c84-5cceadca3f45	2016-11-11	Warnings	Exact identifier unii: ETJ7Z6XBU4
Thyrotox	CHONDRUS CRISPUS, FUCUS VESICULOSUS, THYROIDINUM, BELLADONNA, CALCAREA CARBONICA, CONIUM MACULATUM, IODIUM, KALI CARBONICUM, PHOSPHORUS, PULSATILLA (VULGARIS), SILICEA	BioActive Nutritional, Inc.	e229a260-13f3-4136-b325-9a8954f8a327	2016-08-10	Warnings	Exact identifier unii: ETJ7Z6XBU4
Teething	ARNICA MONTANA, TRIFOLIUM PRATENSE, CALCAREA CARBONICA, CALCAREA FLUORICA, CALCAREA PHOSPHORICA, CHAMOMILLA, KREOSOTUM, SILICEA	BioActive Nutritional, Inc.	f39c9feb-f567-43a2-a026-2a581aeeed9d	2016-07-27	Warnings	Exact identifier unii: ETJ7Z6XBU4

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.