niraparib 100 MG (as niraparib tosylate monohydrate 159.3 MG) Oral Tablet

RxCUI
2637449
RxNorm name
niraparib 100 MG (as niraparib tosylate monohydrate 159.3 MG) Oral Tablet
Display name
niraparib 100 MG (as niraparib tosylate monohydrate 159.3 MG) Oral Tablet
Full name
niraparib 100 MG (as niraparib tosylate monohydrate 159.3 MG) Oral Tablet
Term type
SY
Status
DailyMed mapping
Updated
2026-06-04 23:39:17

RxNav Current And Historical NDCs#

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UNII Substances#

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openFDA label cross-check#

Cross-check layer: openFDA label JSON enriches search and identifies hydration gaps. The DailyMed Structured Product Label remains the canonical label presentation on FDA.report. Every label matching the complete exact-identifier union is deduplicated and paginated below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
ZEJULANIRAPARIBGlaxoSmithKline LLCb7f675e2-159c-490c-b6f4-3f16d9492b7d2026-03-27Warnings, Adverse reactionsExact identifier
rxcui: 2637449

DailyMed RxNorm Mappings#

Set ID, RxNorm string, TTY table
Set IDRxNorm stringTTYSPL versionLabelEffective
b7f675e2-159c-490c-b6f4-3f16d9492b7dniraparib 100 MG (as niraparib tosylate monohydrate 159.3 MG) Oral TabletSY9These highlights do not include all the information needed to use ZEJULA safely and effectively. See full prescribing information for ZEJULA. ZEJULA (niraparib) tablets, for oral use Initial U.S. Approval: 201720260327
b7f675e2-159c-490c-b6f4-3f16d9492b7dniraparib 100 MG Oral TabletPSN9These highlights do not include all the information needed to use ZEJULA safely and effectively. See full prescribing information for ZEJULA. ZEJULA (niraparib) tablets, for oral use Initial U.S. Approval: 201720260327
b7f675e2-159c-490c-b6f4-3f16d9492b7dniraparib 100 MG Oral TabletSCD9These highlights do not include all the information needed to use ZEJULA safely and effectively. See full prescribing information for ZEJULA. ZEJULA (niraparib) tablets, for oral use Initial U.S. Approval: 201720260327