FDA.reportPublic FDA data

Lutrate Depot 22.5 MG Injection

RxCUI
2709448
RxNorm name
Lutrate Depot 22.5 MG Injection
Display name
Lutrate Depot 22.5 MG Injection
Full name
Lutrate Depot 22.5 MG Injection
Term type
PSN
Status
DailyMed mapping
Updated
2026-06-04 23:38:54

RxNav Current And Historical NDCs#

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No records found.

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
LUTRATE DEPOTLEUPROLIDE ACETATEAvyxa Pharma, LLC3a6d1373-17d9-4289-b62f-d299ffe558312025-06-03Warnings, Adverse reactionsExact identifier
rxcui: 2709448

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
3a6d1373-17d9-4289-b62f-d299ffe55831Lutrate Depot 22.5 MG Injection [PSN] · leuprolide acetate 22.5 MG Injection [Lutrate] [SBD] · Lutrate Depot 22.5 MG Injection [SY]32These highlights do not include all the information needed to use LUTRATE DEPOT safely and effectively. See full prescribing information for LUTRATE DEPOT. LUTRATE ® DEPOT (leuprolide acetate), for depot suspension Initial U.S. Approval: 201820250603