FDA.reportPublic FDA data

Augtyro 40 MG Oral Capsule

RxCUI
2670655
RxNorm name
Augtyro 40 MG Oral Capsule
Display name
Augtyro 40 MG Oral Capsule
Full name
Augtyro 40 MG Oral Capsule
Term type
SY
Status
DailyMed mapping
Updated
2026-06-04 23:39:29

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
AugtyroREPOTRECTINIBE.R. Squibb & Sons, L.L.C.fb526827-40ba-4462-94cf-179ae3b0cb8a2024-06-13Warnings, Adverse reactionsExact identifier
rxcui: 2670655

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
fb526827-40ba-4462-94cf-179ae3b0cb8aAUGTYRO 40 MG Oral Capsule [PSN] · repotrectinib 40 MG Oral Capsule [Augtyro] [SBD] · Augtyro 40 MG Oral Capsule [SY]35These highlights do not include all the information needed to use AUGTYRO safely and effectively. See full prescribing information for AUGTYRO. AUGTYRO TM (repotrectinib) capsules, for oral use Initial U.S. Approval: 202320240613