FDA.reportPublic FDA data

60 ACTUAT fluticasone propionate 0.055 MG/ACTUAT / salmeterol 0.014 MG/ACTUAT Dry Powder Inhaler [AirDuo]

RxCUI
1918211
RxNorm name
60 ACTUAT fluticasone propionate 0.055 MG/ACTUAT / salmeterol 0.014 MG/ACTUAT Dry Powder Inhaler [AirDuo]
Display name
60 ACTUAT fluticasone propionate 0.055 MG/ACTUAT / salmeterol 0.014 MG/ACTUAT Dry Powder Inhaler [AirDuo]
Full name
60 ACTUAT fluticasone propionate 0.055 MG/ACTUAT / salmeterol 0.014 MG/ACTUAT Dry Powder Inhaler [AirDuo]
Term type
SBD
Status
DailyMed mapping
Updated
2026-06-04 23:39:10

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 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
AirDuo RespiClickFLUTICASONE PROPIONATE AND SALMETEROLTeva Respiratory, LLC9c122b91-a11f-49ca-80bb-3eec5112db872024-02-06Warnings, Adverse reactionsExact identifier
rxcui: 1918211

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
9c122b91-a11f-49ca-80bb-3eec5112db87AirDuo RespiClick 55/14 MCG/INHAL Dry Powder Inhaler, 60 Actuations [PSN] · 60 ACTUAT fluticasone propionate 0.055 MG/ACTUAT / salmeterol 0.014 MG/ACTUAT Dry Powder Inhaler [AirDuo] [SBD] · AirDuo 55/14 (fluticasone propionate 55 MCG / salmeterol 14 MCG (equivalent to salmeterol xinafoate 20.3 MCG)) per ACTUAT Dry Powder Inhaler, 60 ACTUAT [SY] · AirDuo RespiClick 55/14 Dry Powder Inhaler, 60 ACTUAT [SY]416These highlights do not include all the information needed to use AIRDUO ® RESPICLICK ® safely and effectively. See full prescribing information for AIRDUO RESPICLICK. AIRDUO RESPICLICK (fluticasone propionate and salmeterol) inhalation powder, for oral inhalation use Initial U.S. Approval: 200020240206