FDA.reportPublic FDA data

Oxbryta 300 MG Tablet for Oral Suspension

RxCUI
2588074
RxNorm name
Oxbryta 300 MG Tablet for Oral Suspension
Display name
Oxbryta 300 MG Tablet for Oral Suspension
Full name
Oxbryta 300 MG Tablet for Oral Suspension
Term type
SY
Status
DailyMed mapping
Updated
2026-06-04 23:38:54

RxNav Current And Historical NDCs#

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UNII Substances#

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openFDA label cross-check#

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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: 2588074

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 300 MG Tablet for Oral Suspension [PSN] · voxelotor 300 MG Tablet for Oral Suspension [Oxbryta] [SBD] · Oxbryta 300 MG Tablet for Oral Suspension [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