FDA.reportPublic FDA data

abiraterone acetate 125 MG Oral Tablet [Yonsa]

RxCUI
2046585
RxNorm name
abiraterone acetate 125 MG Oral Tablet [Yonsa]
Display name
abiraterone acetate 125 MG Oral Tablet [Yonsa]
Full name
abiraterone acetate 125 MG Oral Tablet [Yonsa]
Term type
SBD
Status
DailyMed mapping
Updated
2026-06-04 23:39:18

RxNav Current And Historical NDCs#

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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.

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Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
YONSAABIRATERONE ACETATESun Pharmaceutical Industries, Inc.b8967e10-f768-47ce-ac9e-2324c83901322026-06-08Warnings, Adverse reactionsExact identifier
rxcui: 2046585

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
b8967e10-f768-47ce-ac9e-2324c8390132Yonsa 125 MG Oral Tablet [PSN] · abiraterone acetate 125 MG Oral Tablet [Yonsa] [SBD] · Yonsa 125 MG Oral Tablet [SY]313These highlights do not include all the information needed to use YONSA safely and effectively. See full prescribing information for YONSA. YONSA ® (abiraterone acetate) tablets, for oral use Initial U.S. Approval: 201120260521