bevacizumab-bvzr 100 MG in 4 ML Injection

RxCUI
2268039
RxNorm name
bevacizumab-bvzr 100 MG in 4 ML Injection
Display name
bevacizumab-bvzr 100 MG in 4 ML Injection
Full name
bevacizumab-bvzr 100 MG in 4 ML Injection
Term type
PSN
Status
DailyMed mapping
Updated
2026-06-04 23:39:14

Purple Book Biologic Products#

BLA, Proprietary name, Proper name table
BLAProprietary nameProper nameLicense typeStatusLatest source
761099Zirabevbevacizumab-bvzr351(k) BiosimilarRx2026-07-01

RxNav Current And Historical NDCs#

RxNav current and historical NDC rows page 1 of 1 · 0 matching rows.

No records found.

UNII Substances#

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

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
ZirabevBEVACIZUMAB-BVZRPfizer Laboratories Div Pfizer Incaa27acbd-d117-4350-aeee-17bc2e2c0ca42026-07-21Warnings, Adverse reactionsExact identifier
rxcui: 2268039

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
aa27acbd-d117-4350-aeee-17bc2e2c0ca4bevacizumab-bvzr 100 MG in 4 ML Injection [PSN] · 4 ML bevacizumab-bvzr 25 MG/ML Injection [SCD] · bevacizumab-bvzr 100 MG per 4 ML Injection [SY] · bevacizumab-bvzr 25 MG/ML per 4 ML Injection [SY]412These highlights do not include all the information needed to use ZIRABEV safely and effectively. See full prescribing information for ZIRABEV. ZIRABEV™ (bevacizumab-bvzr) injection, for intravenous use Initial U.S. Approval: 2019 ZIRABEV (bevacizumab-bvzr) is biosimilar Biosimilar means that the biological product is approved based on data demonstrating that it is highly similar to an FDA-approved biological product, known as a reference product, and that there are no clinically meaningful differences betw20250805