1.7 ML denosumab-bnht 70 MG/ML Injection

RxCUI
2717542
RxNorm name
1.7 ML denosumab-bnht 70 MG/ML Injection
Display name
1.7 ML denosumab-bnht 70 MG/ML Injection
Full name
1.7 ML denosumab-bnht 70 MG/ML Injection
Term type
SCD
Status
DailyMed mapping
Updated
2026-06-04 23:38:56

Purple Book Biologic Products#

BLA, Proprietary name, Proper name table
BLAProprietary nameProper nameLicense typeStatusLatest source
761398Conexxencedenosumab-bnht351(k) InterchangeableRx2026-07-01

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
BOMYNTRADENOSUMABFresenius Kabi USA, LLC49d25732-e05d-47e4-98cb-67df04796d4b2025-03-31Warnings, Adverse reactionsExact identifier
rxcui: 2717542

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
49d25732-e05d-47e4-98cb-67df04796d4bdenosumab-bnht 120 MG in 1.7 ML Injection [PSN] · 1.7 ML denosumab-bnht 70 MG/ML Injection [SCD] · denosumab-bnht 120 MG per 1.7 ML Injection [SY] · denosumab-bnht 70 MG/ML per 1.7 ML Injection [SY]43These highlights do not include all the information needed to use BOMYNTRA safely and effectively. See full prescribing information for BOMYNTRA. BOMYNTRA (denosumab-bnht) injection, for subcutaneous use Initial U.S. Approval: 2025 BOMYNTRA (denosumab-bnht) 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 betw20250331