FDA.reportPublic FDA data

NDC 55111-233 - 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
55111-233
Package NDCs from labels
55111-233-30, 55111-233-01, 55111-233-05
Manufacturer
Dr. Reddy's Laboratories Limited
Effective date
2007-01-01
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Meloxicam - Dr. Reddy's Laboratories LimitedDr. Reddy's Laboratories Limited2007-01-01HUMAN PRESCRIPTION DRUG LABELING

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
55111-233-01Meloxicam100 in 1 BOTTLETABLET1001
55111-233-05Meloxicam500 in 1 BOTTLETABLET5001
55111-233-30Meloxicam30 in 1 BOTTLETABLET301

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
55111-233MELOXICAM (MELOXICAM) TABLET [DR. REDDY'S LABORATORIES LIMITED]13 package rows20070105_4EC9BF84-D0B0-4092-8E3D-C67CCFB2780B.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
55111-233-01EA - Each55111-233c6b26716-beaa-4ff3-a694-f911147a8af412013-02-13

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
meloxicamACTIVE INGREDIENTVG2QF83CGLMELOXICAM (MELOXICAM) TABLET [DR. REDDY'S LABORATORIES LIMITED]1
meloxicamACTIVE MOIETYVG2QF83CGLMELOXICAM (MELOXICAM) TABLET [DR. REDDY'S LABORATORIES LIMITED]1
colloidal silicon dioxideINACTIVE INGREDIENTMELOXICAM (MELOXICAM) TABLET [DR. REDDY'S LABORATORIES LIMITED]1
crospovidoneINACTIVE INGREDIENTMELOXICAM (MELOXICAM) TABLET [DR. REDDY'S LABORATORIES LIMITED]1
lactose monohydrateINACTIVE INGREDIENTMELOXICAM (MELOXICAM) TABLET [DR. REDDY'S LABORATORIES LIMITED]1
magnesium stearateINACTIVE INGREDIENT70097M6I30MELOXICAM (MELOXICAM) TABLET [DR. REDDY'S LABORATORIES LIMITED]1
microcrystalline celluloseINACTIVE INGREDIENTMELOXICAM (MELOXICAM) TABLET [DR. REDDY'S LABORATORIES LIMITED]1
povidoneINACTIVE INGREDIENTMELOXICAM (MELOXICAM) TABLET [DR. REDDY'S LABORATORIES LIMITED]1
sodium citrate dihydrateINACTIVE INGREDIENTB22547B95KMELOXICAM (MELOXICAM) TABLET [DR. REDDY'S LABORATORIES LIMITED]1

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 3 of 6 · 115 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
meloxicamMELOXICAMNorthwind Health Company, LLC3ce43f4a-c525-4ce1-b328-514b3912e3052026-01-01Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 152695
meloxicamMELOXICAMNorthwind Health Company, LLC820f143f-4b0c-4466-be9a-212dab9d984b2026-01-01Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 311486
MELOXICAMMELOXICAMNorthwind Health Company, LLCf2b42bdc-47e1-19c5-e053-2a95a90a18282026-01-01Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 311486
MELOXICAMMELOXICAMNorthwind Health Company, LLCf31d181a-33cb-560f-e053-2995a90abbd92026-01-01Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 152695
MeloxicamMELOXICAMChartwell RX, LLC8bd53770-7077-49c7-8215-73a17a20ea702025-12-17Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 311486
rxcui: 152695
MELOXICAMMELOXICAMAiPing Pharmaceutical, Incac58edaa-4aba-4fa8-9ccd-f33477aee2182025-12-12Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 311486
rxcui: 152695
MELOXICAMMELOXICAMXLCare Pharmaceuticals, Inc.702a4aa6-a588-48db-9cc5-74ae417f95872025-12-12Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 311486
rxcui: 152695
MeloxicamMELOXICAMAdvanced Rx of Tennessee, LLC445d7cbf-bd3e-a54f-e063-6294a90a67a52025-12-05Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 311486
MeloxicamMELOXICAMAdvanced Rx of Tennessee, LLC445dc4f6-daac-e2f1-e063-6394a90a0ca52025-12-05Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 311486
meloxicamMELOXICAMPHOENIX RX LLC438311de-78e7-8bd9-e063-6394a90a79322025-12-05Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 311486
MeloxicamMELOXICAMAdvanced Rx of Tennessee, LLC453c5328-090e-0159-e063-6394a90a06b72025-12-05Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 311486
meloxicamMELOXICAMQPharma, Inc.20ec4646-9d1c-41c9-93f6-754b3a4f234f2025-12-05Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 152695
meloxicamMELOXICAMA-S Medication Solutions67974608-326e-4e62-8430-6fbc14d1d69b2025-12-04Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 152695
meloxicamMELOXICAMNuCare Pharmaceuticals,Inc.87ef5a9b-2dd1-2ef9-e053-2995a90a51492025-12-04Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 152695
meloxicamMELOXICAMQPharma, Inc.14e7472a-24fe-4ae1-abc7-c2972ce8cd742025-12-04Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 311486
meloxicamMELOXICAMA-S Medication Solutions11984306-9b71-4c2a-81bc-8942966810be2025-12-04Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 152695
meloxicamMELOXICAMPHOENIX RX LLC3ff222f1-3fe2-9591-e063-6394a90a349f2025-09-29Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 152695
MeloxicamMELOXICAMAmerican Health Packaging937ea2ca-6b8c-4c80-9926-f4de7c8f56432025-09-23Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 152695
MeloxicamMELOXICAMAvPAKee8df8fa-d08a-8c8b-f048-813e5022a1012025-09-16Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 311486
rxcui: 152695
meloxicamMELOXICAMPHOENIX RX LLC3ede6724-d9be-5b44-e063-6294a90afbaa2025-09-15Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 152695

Reported adverse events (FAERS/openFDA)#

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