FDA.reportPublic FDA data

voxelotor 500 MG Oral Tablet [Oxbryta]

RxCUI
2265689
RxNorm name
voxelotor 500 MG Oral Tablet [Oxbryta]
Display name
voxelotor 500 MG Oral Tablet [Oxbryta]
Full name
voxelotor 500 MG Oral Tablet [Oxbryta]
Term type
SBD
Status
DailyMed mapping
Updated
2026-06-04 23:38:54

RxNav Current And Historical NDCs#

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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
OXBRYTAVOXELOTORGlobal Blood Therapeutics, Inc, A subsidiary of Pfizer Inc.3c557fac-29ec-483f-b691-8a935d4decc32023-12-26Warnings, Adverse reactionsExact identifier
rxcui: 2265689

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
3c557fac-29ec-483f-b691-8a935d4decc3OXBRYTA 500 MG Oral Tablet [PSN] · voxelotor 500 MG Oral Tablet [Oxbryta] [SBD] · Oxbryta 500 MG Oral Tablet [SY]313These highlights do not include all the information needed to use OXBRYTA safely and effectively. See full prescribing information for OXBRYTA. OXBRYTA ® (voxelotor) tablets, for oral use OXBRYTA ® (voxelotor) tablets for oral suspension Initial U.S. Approval: 201920231226