FDA.reportPublic FDA data

14 ACTUAT fluticasone furoate 0.2 MG/ACTUAT Dry Powder Inhaler

RxCUI
1547666
RxNorm name
14 ACTUAT fluticasone furoate 0.2 MG/ACTUAT Dry Powder Inhaler
Display name
14 ACTUAT fluticasone furoate 0.2 MG/ACTUAT Dry Powder Inhaler
Full name
14 ACTUAT fluticasone furoate 0.2 MG/ACTUAT Dry Powder Inhaler
Term type
SCD
Status
DailyMed mapping
Updated
2026-06-04 23:38:58

RxNav Current And Historical NDCs#

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No records found.

UNII Substances#

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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
Arnuity ElliptaFLUTICASONE FUROATEGlaxoSmithKline LLC50f193ee-1691-486d-9370-a664df63695c2023-10-18Warnings, Adverse reactionsExact identifier
rxcui: 1547666

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
50f193ee-1691-486d-9370-a664df63695cfluticasone furoate 200 MCG/INHAL Dry Powder Inhaler, 14 Blisters [PSN] · 14 ACTUAT fluticasone furoate 0.2 MG/ACTUAT Dry Powder Inhaler [SCD] · fluticasone furoate 200 MCG/ACTUAT Dry Powder Inhaler, 14 ACTUAT [SY]317These highlights do not include all the information needed to use ARNUITY ELLIPTA safely and effectively. See full prescribing information for ARNUITY ELLIPTA. ARNUITY ELLIPTA (fluticasone furoate inhalation powder), for oral inhalation use Initial U.S. Approval: 201420231018