FDA.reportPublic FDA data

pemivibart 500 MG per 4 ML Injection (EUA)

RxCUI
2677805
RxNorm name
pemivibart 500 MG per 4 ML Injection (EUA)
Display name
pemivibart 500 MG per 4 ML Injection (EUA)
Full name
pemivibart 500 MG per 4 ML Injection (EUA)
Term type
SY
Status
DailyMed mapping
Updated
2026-06-04 23:38:47

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
pemgardaPEMIVIBARTInvivyd, Inc0bdc20a9-791f-9a06-e063-6394a90a84cc2025-09-12Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 2677805

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
0bdc20a9-791f-9a06-e063-6394a90a84ccpemivibart 500 MG in 4 ML Injection (EUA) [PSN] · 4 ML pemivibart 125 MG/ML Injection [SCD] · pemivibart 500 MG per 4 ML Injection (EUA) [SY]310FACT SHEET FOR HEALTHCARE PROVIDERS: EMERGENCY USE AUTHORIZATION OF PEMGARDA (PEMIVIBART): These highlights do not include all the information needed to use see full prescribing information for and Initial U.S. Approval20250912