FDA.reportPublic FDA data

0.5 ML leuprolide acetate 60 MG/ML Prefilled Syringe [Vabrinty]

RxCUI
2723399
RxNorm name
0.5 ML leuprolide acetate 60 MG/ML Prefilled Syringe [Vabrinty]
Display name
0.5 ML leuprolide acetate 60 MG/ML Prefilled Syringe [Vabrinty]
Full name
0.5 ML leuprolide acetate 60 MG/ML Prefilled Syringe [Vabrinty]
Term type
SBD
Status
DailyMed mapping
Updated
2026-06-04 23:38:45

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
VabrintyLEUPROLIDE ACETATEURONOVA PHARMACEUTICALS, INC.008776cc-83f1-4f8c-819b-6471425da15f2026-04-30Warnings, Adverse reactionsExact identifier
rxcui: 2723399

DailyMed RxNorm Mappings#

Set ID, RxNorm string, TTY table
Set IDRxNorm stringTTYSPL versionLabelEffective
008776cc-83f1-4f8c-819b-6471425da15f0.5 ML leuprolide acetate 60 MG/ML Prefilled Syringe [Vabrinty]SBD9These highlights do not include all the information needed to use VABRINTY™ safely and effectively. See full prescribing information for VABRINTY. VABRINTY (leuprolide acetate) for injectable suspension, for subcutaneous use Initial U.S. Approval: 200220250601
008776cc-83f1-4f8c-819b-6471425da15fVabrinty 30 MG in 0.5 ML (4 month) Prefilled SyringePSN9These highlights do not include all the information needed to use VABRINTY™ safely and effectively. See full prescribing information for VABRINTY. VABRINTY (leuprolide acetate) for injectable suspension, for subcutaneous use Initial U.S. Approval: 200220250601
008776cc-83f1-4f8c-819b-6471425da15fVabrinty 30 MG per 0.5 ML Prefilled SyringeSY9These highlights do not include all the information needed to use VABRINTY™ safely and effectively. See full prescribing information for VABRINTY. VABRINTY (leuprolide acetate) for injectable suspension, for subcutaneous use Initial U.S. Approval: 200220250601