ponesimod 20 MG Oral Tablet

RxCUI
2532318
RxNorm name
ponesimod 20 MG Oral Tablet
Display name
ponesimod 20 MG Oral Tablet
Full name
ponesimod 20 MG Oral Tablet
Term type
SCD
Status
DailyMed mapping
Updated
2026-06-04 23:39:00

RxNav Current And Historical NDCs#

RxNav current and historical NDC rows page 1 of 1 · 0 matching rows.

No records found.

UNII Substances#

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No records found.

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 · 2 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
PONVORYPONESIMODVanda Pharmaceuticals Inc.0c025ba8-ba51-272e-e063-6294a90ad1202025-12-04Warnings, Adverse reactionsExact identifier
rxcui: 2532318
PONVORYPONESIMODJanssen Pharmaceuticals, Inc5be69660-738c-4db7-b0d4-517aa873dc412025-04-25Warnings, Adverse reactionsExact identifier
rxcui: 2532318

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
5be69660-738c-4db7-b0d4-517aa873dc41ponesimod 20 MG Oral Tablet [PSN] · ponesimod 20 MG Oral Tablet [SCD]213These highlights do not include all the information needed to use PONVORY safely and effectively. See full prescribing information for PONVORY. PONVORY ® (ponesimod) tablets, for oral use Initial U.S. Approval: 202120250425
0c025ba8-ba51-272e-e063-6294a90ad120ponesimod 20 MG Oral Tablet [PSN] · ponesimod 20 MG Oral Tablet [SCD]24These highlights do not include all the information needed to use PONVORY safely and effectively. See full prescribing information for PONVORY. PONVORY ® (ponesimod) tablets, for oral use Initial U.S. Approval: 202120251204