FDA.reportPublic FDA data

1 ML tildrakizumab-asmn 100 MG/ML Prefilled Syringe [Ilumya]

RxCUI
2053458
RxNorm name
1 ML tildrakizumab-asmn 100 MG/ML Prefilled Syringe [Ilumya]
Display name
1 ML tildrakizumab-asmn 100 MG/ML Prefilled Syringe [Ilumya]
Full name
1 ML tildrakizumab-asmn 100 MG/ML Prefilled Syringe [Ilumya]
Term type
SBD
Status
DailyMed mapping
Updated
2026-06-04 23:39:20

Purple Book Biologic Products#

BLA, Proprietary name, Proper name table
BLAProprietary nameProper nameLicense typeStatusLatest source
761067Ilumyatildrakizumab-asmn351(a)Rx2026-08-01

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
ILUMYATILDRAKIZUMAB-ASMNSun Pharmaceutical Industries, Inc.c6a322bb-51b9-4f0e-8642-62a9682ffcde2026-07-29Warnings, Adverse reactionsExact identifier
rxcui: 2053458

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
c6a322bb-51b9-4f0e-8642-62a9682ffcdeILUMYA 100 MG in 1 ML Prefilled Syringe [PSN] · 1 ML tildrakizumab-asmn 100 MG/ML Prefilled Syringe [Ilumya] [SBD] · 1 ML Ilumya 100 MG/ML Prefilled Syringe [SY] · Ilumya 100 MG per 1 ML Prefilled Syringe [SY]418These highlights do not include all the information needed to use ILUMYA safely and effectively. See full prescribing information for ILUMYA. ILUMYA ® (tildrakizumab-asmn) injection, for subcutaneous use Initial U.S. Approval: 201820251225