Imkeldi 80 MG/ML Oral Solution

RxCUI
2699837
RxNorm name
Imkeldi 80 MG/ML Oral Solution
Display name
Imkeldi 80 MG/ML Oral Solution
Full name
Imkeldi 80 MG/ML Oral Solution
Term type
SY
Status
DailyMed mapping
Updated
2026-06-04 23:38:50

RxNav Current And Historical NDCs#

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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.

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Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
IMKELDIIMATINIB ORALShorla Oncology Inc.,26658bb7-9ba1-a10e-e063-6394a90a172e2024-12-05Warnings, Adverse reactionsExact identifier
rxcui: 2699837

DailyMed RxNorm Mappings#

Set ID, RxNorm string, TTY table
Set IDRxNorm stringTTYSPL versionLabelEffective
26658bb7-9ba1-a10e-e063-6394a90a172eImkeldi 80 MG/ML Oral SolutionSY2These highlights do not include all the information needed to use IMKELDI safely and effectively. See full prescribing information for IMKELDI. IMKELDI (imatinib) oral solution Initial U.S. Approval: 200120241205
26658bb7-9ba1-a10e-e063-6394a90a172eImkeldi 80 MG (equivalent to 95.57 MG imatinib mesylate) per 1 ML Oral SolutionSY2These highlights do not include all the information needed to use IMKELDI safely and effectively. See full prescribing information for IMKELDI. IMKELDI (imatinib) oral solution Initial U.S. Approval: 200120241205
26658bb7-9ba1-a10e-e063-6394a90a172eimatinib 80 MG/ML Oral Solution [Imkeldi]SBD2These highlights do not include all the information needed to use IMKELDI safely and effectively. See full prescribing information for IMKELDI. IMKELDI (imatinib) oral solution Initial U.S. Approval: 200120241205
26658bb7-9ba1-a10e-e063-6394a90a172eImkeldi 80 MG/mL Oral SolutionPSN2These highlights do not include all the information needed to use IMKELDI safely and effectively. See full prescribing information for IMKELDI. IMKELDI (imatinib) oral solution Initial U.S. Approval: 200120241205