FDA.reportPublic FDA data

1 ML testosterone cypionate 200 MG/ML Prefilled Syringe

RxCUI
2694309
RxNorm name
1 ML testosterone cypionate 200 MG/ML Prefilled Syringe
Display name
1 ML testosterone cypionate 200 MG/ML Prefilled Syringe
Full name
1 ML testosterone cypionate 200 MG/ML Prefilled Syringe
Term type
SCD
Status
DailyMed mapping
Updated
2026-06-04 23:38:50

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
AZMIROTESTOSTERONE CYPIONATEAzurity Pharmaceuticals, Inc.235b5625-570d-3fba-e063-6394a90aa2d12025-07-25Warnings, Adverse reactionsExact identifier
rxcui: 2694309

DailyMed RxNorm Mappings#

Set ID, RxNorm string, TTY table
Set IDRxNorm stringTTYSPL versionLabelEffective
235b5625-570d-3fba-e063-6394a90aa2d11 ML testosterone cypionate 200 MG/ML Prefilled SyringeSCD3These highlights do not include all the information needed to use AZMIRO safely and effectively. See full prescribing information for AZMIRO. AZMIRO TM (testosterone cypionate) injection, for intramuscular use, CIII Initial U.S. Approval: 195320250725
235b5625-570d-3fba-e063-6394a90aa2d1testosterone cypionate 200 MG per 1 ML Prefilled SyringeSY3These highlights do not include all the information needed to use AZMIRO safely and effectively. See full prescribing information for AZMIRO. AZMIRO TM (testosterone cypionate) injection, for intramuscular use, CIII Initial U.S. Approval: 195320250725
235b5625-570d-3fba-e063-6394a90aa2d1testosterone cypionate 200 MG in 1 ML Prefilled SyringePSN3These highlights do not include all the information needed to use AZMIRO safely and effectively. See full prescribing information for AZMIRO. AZMIRO TM (testosterone cypionate) injection, for intramuscular use, CIII Initial U.S. Approval: 195320250725