FDA.reportPublic FDA data

Advair Diskus 500/50 Dry Powder Inhaler, 14 ACTUAT

RxCUI
896222
RxNorm name
Advair Diskus 500/50 Dry Powder Inhaler, 14 ACTUAT
Display name
Advair Diskus 500/50 Dry Powder Inhaler, 14 ACTUAT
Full name
Advair Diskus 500/50 Dry Powder Inhaler, 14 ACTUAT
Term type
SY
Status
DailyMed mapping
Updated
2026-06-04 23:38:57

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.

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Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
ADVAIR DISKUSFLUTICASONE PROPIONATE AND SALMETEROLGlaxoSmithKline LLC4eeb5f6a-593f-4a9e-9692-adefa2caf8fc2026-03-26Warnings, Adverse reactionsExact identifier
rxcui: 896222

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
4eeb5f6a-593f-4a9e-9692-adefa2caf8fcADVAIR DISKUS 500/50 MCG/INHAL Dry Powder Inhaler, 14 Blisters [PSN] · 14 ACTUAT fluticasone propionate 0.5 MG/ACTUAT / salmeterol 0.05 MG/ACTUAT Dry Powder Inhaler [Advair] [SBD] · Advair Diskus 500/50 (fluticasone propionate 500 MCG / salmeterol 50 MCG (salmeterol xinafoate 72.5 MCG)) per ACTUAT Dry Powder Inhaler, 14 ACTUAT [SY] · Advair Diskus 500/50 Dry Powder Inhaler, 14 ACTUAT [SY]432These highlights do not include all the information needed to use ADVAIR DISKUS safely and effectively. See full prescribing information for ADVAIR DISKUS. ADVAIR DISKUS (fluticasone propionate and salmeterol inhalation powder), for oral inhalation use Initial U.S. Approval: 200020260326