NDC 68071-2184-05 - MELOXICAM

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: 68071-2184
Requested NDC: 68071-2184-05
Package NDCs from labels: 68071-2184-3, 68071-2184-9, 68071-2184-5, 68071-2184-05
Manufacturer: NuCare Pharmaceuticals, Inc.
Effective date: 2024-08-19
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
MELOXICAM - NuCare Pharmaceuticals, Inc.	NuCare Pharmaceuticals, Inc.	2024-08-19	HUMAN PRESCRIPTION DRUG LABEL

FDA-Initiated Inactive NDC Indexing#

Effective, Related label table
Effective	Related label
2023-06-19	These highlights do not include all the information needed to use MELOXICAM TABLETS safely and effectively. See full prescribing information for MELOXICAM TABLETS. Initial U.S. Approval: 2000
2023-01-30	These highlights do not include all the information needed to use MELOXICAM TABLETS safely and effectively. See full prescribing information for MELOXICAM TABLETS. Initial U.S. Approval: 2000
2020-10-12	These highlights do not include all the information needed to use MELOXICAM TABLETS safely and effectively. See full prescribing information for MELOXICAM TABLETS. Initial U.S. Approval: 2000
2020-01-31	These highlights do not include all the information needed to use MELOXICAM TABLETS safely and effectively. See full prescribing information for MELOXICAM TABLETS. Initial U.S. Approval: 2000

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
68071-2184-3	MELOXICAM	30 in 1 BOTTLE	TABLET	30	6
68071-2184-5	MELOXICAM	15 in 1 BOTTLE	TABLET	15	6
68071-2184-9	MELOXICAM	90 in 1 BOTTLE	TABLET	90	6

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
68071-2184	MELOXICAM TABLET [NUCARE PHARMACEUTICALS, INC.]	6	Current NDC, Legacy NDC, 3 package rows	20240820_43ca4ab6-7d52-2954-e054-00144ff88e88.zip

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 · 121 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Meloxicam	MELOXICAM	Exelan Pharmaceuticals Inc.	dfaac71c-dcc5-4b57-bf3b-616fccab96de	2018-09-19	Boxed warning, Warnings, Adverse reactions	Exact identifier rxcui: 311486 rxcui: 152695 unii: VG2QF83CGL

Reported adverse events (FAERS/openFDA)#

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