bortezomib 1 MG Injection

RxCUI
2601542
RxNorm name
bortezomib 1 MG Injection
Display name
bortezomib 1 MG Injection
Full name
bortezomib 1 MG Injection
Term type
SCD
Status
DailyMed mapping
Updated
2026-06-04 23:39:21

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 · 2 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
BortezomibBORTEZOMIBGland Pharma Limitedcd698074-da21-4b53-8f6b-241535a8d5982026-01-08Warnings, Adverse reactionsExact identifier
rxcui: 2601542
BORTEZOMIBBORTEZOMIBHospira, Inc.9fdf6169-699f-40eb-bda1-760253062b3c2023-02-27Warnings, Adverse reactionsExact identifier
rxcui: 2601542

DailyMed RxNorm Mappings#

unique DailyMed labels mapped to this RxNorm concept page 1 of 1 · 2 matching rows.

Set ID, RxNorm mappings, Terms table
Set IDRxNorm mappingsTermsSPL versionLabelEffective
cd698074-da21-4b53-8f6b-241535a8d598bortezomib 1 MG Injection [PSN] · bortezomib 1 MG Injection [SCD]24These highlights do not include all the information needed to use BORTEZOMIB FOR INJECTION safely and effectively. See full prescribing information for BORTEZOMIB FOR INJECTION. BORTEZOMIB for injection, for subcutaneous or intravenous use Initial U.S. Approval: 200320260108
9fdf6169-699f-40eb-bda1-760253062b3cbortezomib 1 MG Injection [PSN] · bortezomib 1 MG Injection [SCD]23These highlights do not include all the information needed to use BORTEZOMIB FOR INJECTION safely and effectively. See full prescribing information for BORTEZOMIB FOR INJECTION. BORTEZOMIB for injection, for subcutaneous or intravenous use Initial U.S. Approval: 200320230227