FDA.reportPublic FDA data

evolocumab 420 in 3.5 ML Cartridge

RxCUI
1801319
RxNorm name
evolocumab 420 in 3.5 ML Cartridge
Display name
evolocumab 420 in 3.5 ML Cartridge
Full name
evolocumab 420 in 3.5 ML Cartridge
Term type
PSN
Status
DailyMed mapping
Updated
2026-06-04 23:39:21

Purple Book Biologic Products#

BLA, Proprietary name, Proper name table
BLAProprietary nameProper nameLicense typeStatusLatest source
125522Repathaevolocumab351(a)Rx2026-10-01

RxNav Current And Historical NDCs#

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No records found.

UNII Substances#

UNII substance links page 1 of 1 · 0 matching rows.

No records found.

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
cd61e902-166d-4aa6-9f3c-a18c1008d07eevolocumab 420 in 3.5 ML Cartridge [PSN] · 3.5 ML evolocumab 120 MG/ML Cartridge [SCD] · evolocumab 420 per 3.5 ML Cartridge [SY]327These highlights do not include all the information needed to use REPATHA ® safely and effectively. See full prescribing information for REPATHA. REPATHA (evolocumab) injection, for subcutaneous use Initial U.S. Approval: 201520260122