Orilissa 200 MG Oral Tablet

RxCUI
2049862
RxNorm name
Orilissa 200 MG Oral Tablet
Display name
Orilissa 200 MG Oral Tablet
Full name
Orilissa 200 MG Oral Tablet
Term type
SY
Status
DailyMed mapping
Updated
2026-06-04 23:39:14

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
OrilissaELAGOLIXAbbVie Inc.a86757b3-09c5-fd3b-1223-244e94f50a662025-12-19Warnings, Adverse reactionsExact identifier
rxcui: 2049862

DailyMed RxNorm Mappings#

Set ID, RxNorm string, TTY table
Set IDRxNorm stringTTYSPL versionLabelEffective
a86757b3-09c5-fd3b-1223-244e94f50a66Orilissa 200 MG Oral TabletSY111These highlights do not include all the information needed to use ORILISSA safely and effectively. See full prescribing information for ORILISSA. ORILISSA ® (elagolix) tablets, for oral use Initial U.S. Approval: 201820251219
a86757b3-09c5-fd3b-1223-244e94f50a66elagolix 200 MG Oral Tablet [Orilissa]SBD111These highlights do not include all the information needed to use ORILISSA safely and effectively. See full prescribing information for ORILISSA. ORILISSA ® (elagolix) tablets, for oral use Initial U.S. Approval: 201820251219
a86757b3-09c5-fd3b-1223-244e94f50a66Orilissa 200 MG Oral TabletPSN111These highlights do not include all the information needed to use ORILISSA safely and effectively. See full prescribing information for ORILISSA. ORILISSA ® (elagolix) tablets, for oral use Initial U.S. Approval: 201820251219