FDA.reportPublic FDA data

diroximel fumarate 231 MG Delayed Release Oral Capsule [Vumerity]

RxCUI
2261794
RxNorm name
diroximel fumarate 231 MG Delayed Release Oral Capsule [Vumerity]
Display name
diroximel fumarate 231 MG Delayed Release Oral Capsule [Vumerity]
Full name
diroximel fumarate 231 MG Delayed Release Oral Capsule [Vumerity]
Term type
SBD
Status
DailyMed mapping
Updated
2026-06-04 23:38:52

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.

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

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
VumerityDIROXIMEL FUMARATEBiogen Inc.2d74414f-6b83-4ea2-9a95-3cecabbce7742025-05-29Warnings, Adverse reactionsExact identifier
rxcui: 2261794

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
2d74414f-6b83-4ea2-9a95-3cecabbce774VUMERITY 231 MG Delayed Release Oral Capsule [PSN] · diroximel fumarate 231 MG Delayed Release Oral Capsule [Vumerity] [SBD] · Vumerity 231 MG Delayed Release Oral Capsule [SY]316These highlights do not include all the information needed to use VUMERITY ® safely and effectively. See full prescribing information for VUMERITY. VUMERITY ® (diroximel fumarate) delayed-release capsules, for oral use Initial U.S. Approval: 201320250529