artemether 20 MG / lumefantrine 120 MG Oral Tablet

RxCUI
847731
RxNorm name
artemether 20 MG / lumefantrine 120 MG Oral Tablet
Display name
artemether 20 MG / lumefantrine 120 MG Oral Tablet
Full name
artemether 20 MG / lumefantrine 120 MG Oral Tablet
Term type
PSN
Status
DailyMed mapping
Updated
2026-06-04 23:39:05

RxNav Current And Historical NDCs#

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No records found.

UNII Substances#

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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 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
COARTEMARTEMETHER AND LUMEFANTRINENovartis Pharmaceuticals Corporation7866ec19-dfac-47d4-a53f-511a12643cbf2026-03-26Warnings, Adverse reactionsExact identifier
rxcui: 847731

Reported adverse events (FAERS/openFDA)#

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

DailyMed RxNorm Mappings#

unique DailyMed labels mapped to this RxNorm concept page 1 of 1 · 2 matching rows.

Set ID, RxNorm mappings, Terms table
Set IDRxNorm mappingsTermsSPL versionLabelEffective
7866ec19-dfac-47d4-a53f-511a12643cbfartemether 20 MG / lumefantrine 120 MG Oral Tablet [PSN] · artemether 20 MG / lumefantrine 120 MG Oral Tablet [SCD]225These highlights do not include all the information needed to use COARTEM Tablets safely and effectively. See full prescribing information for COARTEM Tablets. COARTEM ® (artemether and lumefantrine) tablets, for oral use Initial U.S. Approval: 200920260326
66e02264-6917-4185-9c36-9dc64eaaeb23artemether 20 MG / lumefantrine 120 MG Oral Tablet [PSN] · artemether 20 MG / lumefantrine 120 MG Oral Tablet [SCD]21These highlights do not include all the information needed to use COARTEM Tablets safely and effectively. See full prescribing information for COARTEM Tablets. COARTEM ® (artemether/lumefantrine) Tablets Initial U.S. Approval: 200920170828