NDC 50090-4665-01 - Aripiprazole

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: 50090-4665
Requested NDC: 50090-4665-01
Package NDCs from labels: 50090-4665-0, 50090-4665-1, 50090-4665-01
Manufacturer: A-S Medication Solutions
Effective date: 2024-06-05
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Aripiprazole - A-S Medication Solutions	A-S Medication Solutions	2024-06-05	Human Prescription Drug Label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Related label table
NDC	Effective	Related label
50090-4665-0	2023-02-07	These highlights do not include all the information needed to use ARIPIPRAZOLE TABLETS safely and effectively. See full prescribing information for ARIPIPRAZOLE TABLETS. ARIPIPRAZOLE tablets, for oral use Initial U.S. Approval: 2002
50090-4665-1	2023-02-07	These highlights do not include all the information needed to use ARIPIPRAZOLE TABLETS safely and effectively. See full prescribing information for ARIPIPRAZOLE TABLETS. ARIPIPRAZOLE tablets, for oral use Initial U.S. Approval: 2002
50090-4665-0	2023-01-30	These highlights do not include all the information needed to use ARIPIPRAZOLE TABLETS safely and effectively. See full prescribing information for ARIPIPRAZOLE TABLETS. ARIPIPRAZOLE tablets, for oral use Initial U.S. Approval: 2002
50090-4665-1	2023-01-30	These highlights do not include all the information needed to use ARIPIPRAZOLE TABLETS safely and effectively. See full prescribing information for ARIPIPRAZOLE TABLETS. ARIPIPRAZOLE tablets, for oral use Initial U.S. Approval: 2002

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
50090-4665-0	Aripiprazole	30 in 1 BOTTLE	TABLET	30		11
50090-4665-1	Aripiprazole	90 in 1 BOTTLE	TABLET	90		11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
50090-4665	ARIPIPRAZOLE TABLET [A-S MEDICATION SOLUTIONS]	11	Current NDC, Legacy NDC, 2 package rows	20240606_3ab6af7c-3169-46bf-bd3f-697c81bbcede.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
50090-4665-0	EA - Each	50090-4665	4ad0f1c1-9e23-4b56-b8ed-52d47aa89aaf	1	2022-12-07
50090-4665-1	EA - Each	50090-4665	d7f8d195-7cdb-4734-accb-65879cc06fe6	1	2024-07-12

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 7 of 7 · 123 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Aripiprazole	ARIPIPRAZOLE	Proficient Rx LP	dbdc8fbe-c75f-4f17-a2cd-9f23802dcc5d	2019-11-01	Boxed warning, Warnings, Adverse reactions	Exact identifier rxcui: 602964 unii: 82VFR53I78
Aripiprazole	ARIPIPRAZOLE	Exelan Pharmaceuticals, Inc.	705190bf-9f9d-4183-a56b-4eeafeacde59	2018-12-28	Boxed warning, Warnings, Adverse reactions	Exact identifier rxcui: 349547 rxcui: 349553 rxcui: 602964 rxcui: 349545 rxcui: 349490 rxcui: 402131 unii: 82VFR53I78
ARIPIPRAZOLE	ARIPIPRAZOLE	Camber Pharmaceuticals, Inc.	3718e585-06b9-40fd-a3eb-18b6497a4235	2017-08-08	Boxed warning, Warnings, Adverse reactions	Exact identifier rxcui: 349547 rxcui: 349553 rxcui: 602964 rxcui: 349545 rxcui: 349490 rxcui: 402131 unii: 82VFR53I78

Reported adverse events (FAERS/openFDA)#

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