selinexor 60 MG Twice Weekly (120 MG total weekly) Dose Carton Pack, 4 Blister Cards, 6 Tablets Each

RxCUI
2382989
RxNorm name
selinexor 60 MG Twice Weekly (120 MG total weekly) Dose Carton Pack, 4 Blister Cards, 6 Tablets Each
Display name
selinexor 60 MG Twice Weekly (120 MG total weekly) Dose Carton Pack, 4 Blister Cards, 6 Tablets Each
Full name
selinexor 60 MG Twice Weekly (120 MG total weekly) Dose Carton Pack, 4 Blister Cards, 6 Tablets Each
Term type
SY
Status
DailyMed mapping
Updated
2026-06-04 23:39:28

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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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
XPOVIOSELINEXORKaryopharm Therapeutics Inc.f6dd2682-75a6-4863-90a8-a3197f6f78a82026-05-12Warnings, Adverse reactionsExact identifier
rxcui: 2382989

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 · 1 matching rows.

Set ID, RxNorm mappings, Terms table
Set IDRxNorm mappingsTermsSPL versionLabelEffective
f6dd2682-75a6-4863-90a8-a3197f6f78a8{24 (selinexor 20 MG Oral Tablet) } Pack [GPCK] · selinexor 60 MG Twice Weekly (120 MG total weekly) Dose Carton Pack, 20 MG oral Tablet 24 Count Pack [PSN] · selinexor 60 MG Twice Weekly (120 MG total weekly) Dose Carton Pack, 4 Blister Cards, 6 Tablets Each [SY]318These highlights do not include all the information needed to use XPOVIO safely and effectively. See full prescribing information for XPOVIO. XPOVIO ® (selinexor) tablets, for oral use Initial U.S. Approval: 201920260512