FDA.reportPublic FDA data

NDC 59368-397 - 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
59368-397
Package NDCs from labels
59368-397-01
Manufacturer
Praxis, LLC
Effective date
2023-01-01
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Ibuprofen - Praxis, LLCPraxis, LLC2023-01-01HUMAN OTC DRUG LABEL

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 46 of 66 · 1,308 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
IbuprofenIBUPROFENA-S Medication Solutionsb87cf806-1635-44d5-a9de-383081cb37d82024-10-14WarningsExact identifier
unii: WK2XYI10QM
Eye WashWATER SOLUTIONKroger Company354402ad-581d-47e7-9fd3-933bef281ff42024-10-11WarningsExact identifier
unii: 059QF0KO0R
Eye WashWATERHubei Changjian Medical Products Co., Ltd.d57e1c5b-1edc-4a94-88bc-f9ecf347b7ea2024-10-11WarningsExact identifier
unii: 059QF0KO0R
IbuprofenIBUPROFENA-S Medication Solutionsdf0e55d0-617c-4084-984f-ece2f640e7152024-10-11Boxed warning, Warnings, Adverse reactionsExact identifier
unii: WK2XYI10QM
IbuprofenIBUPROFENA-S Medication Solutionsb0917020-f0ec-4d07-8fbf-c1eb909f466b2024-10-10Boxed warning, Warnings, Adverse reactionsExact identifier
unii: WK2XYI10QM
Ibuprofen and famotidineIBUPROFEN AND FAMOTIDINEPar Health USA, LLCb6895176-efb1-472e-8b6f-2987e8e676842024-10-10Boxed warning, Warnings, Adverse reactionsExact identifier
unii: WK2XYI10QM
IbuprofenIBUPROFENA-S Medication Solutionsb365be3a-91ad-46bf-a949-103c81f2359a2024-10-10Boxed warning, Warnings, Adverse reactionsExact identifier
unii: WK2XYI10QM
IbuprofenIBUPROFENWestminster Pharmaceuticals, LLCeeb8312f-7fd9-4c4f-8264-a7e63ff1aa9d2024-10-10Boxed warning, Warnings, Adverse reactionsExact identifier
unii: WK2XYI10QM
IbuprofenIBUPROFENA-S Medication Solutions0ce79e85-0b8b-436e-b895-ea5c02eaf4ba2024-10-10Boxed warning, Warnings, Adverse reactionsExact identifier
unii: WK2XYI10QM
IbuprofenIBUPROFENA-S Medication Solutions8d41cc03-dec6-4949-b7c1-7deb2897e2c42024-10-10Boxed warning, Warnings, Adverse reactionsExact identifier
unii: WK2XYI10QM
IbuprofenIBUPROFENNuCare Pharmaceuticals, Inc.23fb1113-9f1c-88e0-e063-6394a90a44502024-10-08Boxed warning, Warnings, Adverse reactionsExact identifier
unii: WK2XYI10QM
Ibuprofen and famotidineIBUPROFEN AND FAMOTIDINEBryant Ranch Prepackee69d3cb-dc95-410c-a7c8-6623073a923d2024-10-08Boxed warning, Warnings, Adverse reactionsExact identifier
unii: WK2XYI10QM
IbuprofenIBUPROFENP & L Development, LLC1f9c94a6-938a-420f-b90c-36b3791e97ad2024-10-07WarningsExact identifier
unii: WK2XYI10QM
dual action pain relieverACETAMINOPHEN AND IBUPROFENCHAIN DRUG MARKETING ASSOCIATION INC.2397603c-8d87-2e65-e063-6394a90ab73e2024-10-03WarningsExact identifier
unii: WK2XYI10QM
dual action pain relieverACETAMINOPHEN AND IBUPROFENCHAIN DRUG MARKETING ASSOCIATION INC.23994b21-cbc2-5a34-e063-6394a90acfdf2024-10-03WarningsExact identifier
unii: WK2XYI10QM
IbuprofenIBUPROFENProficient Rx LP43ac478c-43db-4136-8fee-4a43b09681e52024-10-02Boxed warning, Warnings, Adverse reactionsExact identifier
unii: WK2XYI10QM
IbuprofenIBUPROFENH E B2f193146-74b2-4941-893d-3d2f5c8ee6592024-10-01WarningsExact identifier
unii: WK2XYI10QM
Ibuprofen 200mgIBUPROFEN 200MGAllegiant Health265e2b47-d14a-45a8-adc0-7214e20571032024-09-30WarningsExact identifier
unii: WK2XYI10QM
Dual Action Pain ReliefACETAMINOPHEN, IBUPROFENTARGET CORPORATIONe680652b-30d8-6009-e053-2995a90abe292024-09-25WarningsExact identifier
unii: WK2XYI10QM
equate ibuprofenIBUPROFENWal-Mart Stores Inc307b0257-d636-416b-828a-f901782e9b102024-09-13WarningsExact identifier
unii: WK2XYI10QM

Reported adverse events (FAERS/openFDA)#

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