FDA.reportPublic FDA data

fluticasone propionate 0.25 MG/ACTUAT Dry Powder Inhaler, 60 ACTUAT

RxCUI
896025
RxNorm name
fluticasone propionate 0.25 MG/ACTUAT Dry Powder Inhaler, 60 ACTUAT
Display name
fluticasone propionate 0.25 MG/ACTUAT Dry Powder Inhaler, 60 ACTUAT
Full name
fluticasone propionate 0.25 MG/ACTUAT Dry Powder Inhaler, 60 ACTUAT
Term type
SY
Status
DailyMed mapping
Updated
2026-06-04 23:38:56

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.

Matched openFDA labels page 1 of 1 · 2 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
FLUTICASONE PROPIONATE DISKUSFLUTICASONE PROPIONATESportpharm LLC348cbd8c-edeb-499c-961d-3aeb5cc2cef12026-07-28Warnings, Adverse reactionsExact identifier
rxcui: 896025
FLUTICASONE PROPIONATE DISKUSFLUTICASONE PROPIONATEPrasco Laboratories44d009ba-d4b8-410f-b2bc-71ab2d05ac9e2023-05-31Warnings, Adverse reactionsExact identifier
rxcui: 896025

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

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
44d009ba-d4b8-410f-b2bc-71ab2d05ac9efluticasone propionate 250 MCG/INHAL Dry Powder Inhaler, 60 Blisters [PSN] · 60 ACTUAT fluticasone propionate 0.25 MG/ACTUAT Dry Powder Inhaler [SCD] · fluticasone propionate 0.25 MG/ACTUAT Dry Powder Inhaler, 60 ACTUAT [SY]34These highlights do not include all the information needed to use Fluticasone Propionate DISKUS safely and effectively. See full prescribing information for Fluticasone Propionate DISKUS. Fluticasone Propionate DISKUS (fluticasone propionate inhalation powder), for oral inhalation use Initial U.S. Approval: 199420230531