FDA.reportPublic FDA data

NDC 51672-2144-01 - Ibuprofen

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
51672-2144
Requested NDC
51672-2144-01
Package NDCs from labels
51672-2144-8, 51672-2144-1, 51672-2144-01
Manufacturer
Sun Pharmaceutical Industries, Inc. | Sun Pharma Canada Inc.
Effective date
2025-07-07
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
IbuprofenSun Pharmaceutical Industries, Inc. | Sun Pharma Canada Inc.2025-07-07HUMAN OTC DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
51672-2144-1Ibuprofen240 mL in 1 BOTTLESUSPENSION2405
51672-2144-1Ibuprofen1 in 1 CARTONSUSPENSION15
51672-2144-8Ibuprofen120 mL in 1 BOTTLESUSPENSION1205
51672-2144-8Ibuprofen1 in 1 CARTONSUSPENSION15

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
51672-2144IBUPROFEN SUSPENSION [-SUN PHARMACEUTICAL INDUSTRIES, INC.]4Current NDC, Legacy NDC, 4 package rows20250406_6cf3328b-da8f-4f6b-8237-16a4d6b9c833.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 84 of 86 · 1,716 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
childrens ibuprofenIBUPROFENH E Be7e2b766-6d05-49e2-9e88-72454b8579352019-12-27WarningsExact identifier
rxcui: 197803
unii: WK2XYI10QM
RenacidinCITRIC ACID, GLUCONOLACTONE AND MAGNESIUM CARBONATEUnited-Guardian, Inc.13a9bbba-db21-4cba-991c-5d8afaf2ed742019-12-17Warnings, Adverse reactionsExact identifier
unii: XF417D3PSL
Ibuprofen 200mgIBUPROFEN 200MGAllegiant Health2e33a153-0a3f-4b88-b193-d63e0b792ccc2019-12-12WarningsExact identifier
unii: WK2XYI10QM
IbuprofenIBUPROFENPuraCap Pharmaceutical LLC73eb763e-ce21-4cff-854f-3297f20f1f612019-12-10WarningsExact identifier
unii: WK2XYI10QM
IbuprofenIBUPROFENPuraCap Pharmaceutical LLC40501966-419a-4ccd-b7c9-5581cbe47a972019-12-10WarningsExact identifier
unii: WK2XYI10QM
IbuprofenIBUPROFENPuraCap Pharmaceutical LLCb6e14f73-1f19-4cfa-8858-136a38ee32d02019-12-10WarningsExact identifier
unii: WK2XYI10QM
IbuprofenIBUPROFENPuraCap Pharmaceutical LLC67e09ad5-e010-4aa1-b86e-9b22331bf33b2019-12-10WarningsExact identifier
unii: WK2XYI10QM
IbuprofenIBUPROFENPuraCap Pharmaceutical LLC24ef6819-f098-4d01-bfe7-6ffa4aa0e6712019-12-10WarningsExact identifier
unii: WK2XYI10QM
Congestion ReliefIBUPROFEN, PHENYLEPHRINE HCLMeijer Distribution Inc84f932b6-0aee-4cf9-b4b9-213560c42c1d2019-12-05WarningsExact identifier
unii: WK2XYI10QM
IbuprofenIBUPROFENHumanwell PuraCap Pharmaceutical (Wuhan) Co., Ltd50bab3b2-f710-46ff-96cd-1ec4d46585292019-11-22WarningsExact identifier
unii: WK2XYI10QM
IbuprofenIBUPROFENHumanwell PuraCap Pharmaceutical (Wuhan) Co., Ltdf42506f7-896c-47a9-a4b1-ed72434d7aa02019-11-22WarningsExact identifier
unii: WK2XYI10QM
IbuprofenIBUPROFENHumanwell PuraCap Pharmaceutical (Wuhan) Co., Ltd58bff8bf-5a4e-4390-9c03-e266d31deb6b2019-11-22WarningsExact identifier
unii: WK2XYI10QM
IbuprofenIBUPROFENHumanwell PuraCap Pharmaceutical (Wuhan) Co., Ltddaf579dc-91d1-4950-b637-c1a34f5542c52019-11-22WarningsExact identifier
unii: WK2XYI10QM
IbuprofenIBUPROFENSam's West, Inc.90c301ad-7bbd-4e21-8054-35596b208cd42019-11-21WarningsExact identifier
unii: WK2XYI10QM
CPDA-1ANTICOAGULANT CITRATE PHOSPHATE DEXTROSE ADENINEFenwal, Inc.e41adb4e-06fb-4141-ba55-50b043f3c9da2019-11-19Exact identifier
unii: XF417D3PSL
CPDA-1ANTICOAGULANT CITRATE PHOSPHATE DEXTROSE ADENINEFenwal, Inc.14445dfd-6041-40cd-a043-3f4da6bcb9c12019-11-18Exact identifier
unii: XF417D3PSL
CPDA-1ANTICOAGULANT CITRATE PHOSPHATE DEXTROSE ADENINEFenwal, Inc.2557199a-5f60-49d8-b093-1e07002112432019-11-18Exact identifier
unii: XF417D3PSL
CPDA-1ANTICOAGULANT CITRATE PHOSPHATE DEXTROSE ADENINEFenwal, Inc.794f724c-87f0-49c1-9b26-c9e4919783132019-11-18Exact identifier
unii: XF417D3PSL
CPDA-1ANTICOAGULANT CITRATE PHOSPHATE DEXTROSE ADENINEFenwal, Inc.5c7d3287-883a-459b-9214-074a583c8a592019-11-18Exact identifier
unii: XF417D3PSL
CPDA-1ANTICOAGULANT CITRATE PHOSPHATE DEXTROSE ADENINEFenwal, Inc.448a1dc5-7a98-4b2f-82af-4b92de05cfc32019-11-18Exact identifier
unii: XF417D3PSL

Reported adverse events (FAERS/openFDA)#

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