upadacitinib 1 MG per 1 ML Oral Solution

RxCUI
2681015
RxNorm name
upadacitinib 1 MG per 1 ML Oral Solution
Display name
upadacitinib 1 MG per 1 ML Oral Solution
Full name
upadacitinib 1 MG per 1 ML Oral Solution
Term type
SY
Status
DailyMed mapping
Updated
2026-06-04 23:38:51

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
RinvoqUPADACITINIBAbbVie Inc.2966aec7-2ef0-923c-d8ff-fe1a957bf0952026-06-30Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 2681015

DailyMed RxNorm Mappings#

Set ID, RxNorm string, TTY table
Set IDRxNorm stringTTYSPL versionLabelEffective
2966aec7-2ef0-923c-d8ff-fe1a957bf095upadacitinib 1 MG per 1 ML Oral SolutionSY100These highlights do not include all the information needed to use RINVOQ / RINVOQ LQ safely and effectively. See full prescribing information for RINVOQ / RINVOQ LQ . RINVOQ ® (upadacitinib) extended-release tablets, for oral use RINVOQ ® LQ (upadacitinib) oral solution Initial U.S. Approval: 201920251023
2966aec7-2ef0-923c-d8ff-fe1a957bf095upadacitinib 1 MG in 1 mL Oral SolutionPSN100These highlights do not include all the information needed to use RINVOQ / RINVOQ LQ safely and effectively. See full prescribing information for RINVOQ / RINVOQ LQ . RINVOQ ® (upadacitinib) extended-release tablets, for oral use RINVOQ ® LQ (upadacitinib) oral solution Initial U.S. Approval: 201920251023
2966aec7-2ef0-923c-d8ff-fe1a957bf095upadacitinib 1 MG/ML Oral SolutionSCD100These highlights do not include all the information needed to use RINVOQ / RINVOQ LQ safely and effectively. See full prescribing information for RINVOQ / RINVOQ LQ . RINVOQ ® (upadacitinib) extended-release tablets, for oral use RINVOQ ® LQ (upadacitinib) oral solution Initial U.S. Approval: 201920251023