Reclast 5 MG per 100 ML Injection

RxCUI
705875
RxNorm name
Reclast 5 MG per 100 ML Injection
Display name
Reclast 5 MG per 100 ML Injection
Full name
Reclast 5 MG per 100 ML Injection
Term type
SY
Status
DailyMed mapping
Updated
2026-06-04 23:38:59

RxNav Current And Historical NDCs#

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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.

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Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
ReclastZOLEDRONIC ACIDSandoz Inc5a9b3737-9ce6-4a89-b76e-6aab79eba9cf2026-02-03Warnings, Adverse reactionsExact identifier
rxcui: 705875

DailyMed RxNorm Mappings#

Set ID, RxNorm string, TTY table
Set IDRxNorm stringTTYSPL versionLabelEffective
5a9b3737-9ce6-4a89-b76e-6aab79eba9cfReclast 5 MG per 100 ML InjectionSY3These highlights do not include all the information needed to use RECLAST safely and effectively. See full prescribing information for RECLAST. RECLAST ® (zoledronic acid) Injection Initial U.S. Approval: 200120260203
5a9b3737-9ce6-4a89-b76e-6aab79eba9cfReclast 5 MG in 100 ML InjectionPSN3These highlights do not include all the information needed to use RECLAST safely and effectively. See full prescribing information for RECLAST. RECLAST ® (zoledronic acid) Injection Initial U.S. Approval: 200120260203
5a9b3737-9ce6-4a89-b76e-6aab79eba9cfReclast 0.05 MG/ML per 100 ML InjectionSY3These highlights do not include all the information needed to use RECLAST safely and effectively. See full prescribing information for RECLAST. RECLAST ® (zoledronic acid) Injection Initial U.S. Approval: 200120260203
5a9b3737-9ce6-4a89-b76e-6aab79eba9cf100 ML zoledronic acid 0.05 MG/ML Injection [Reclast]SBD3These highlights do not include all the information needed to use RECLAST safely and effectively. See full prescribing information for RECLAST. RECLAST ® (zoledronic acid) Injection Initial U.S. Approval: 200120260203