FDA.reportPublic FDA data

Sensor 200 ACTUAT ProAir 0.09 MG/ACTUAT Dry Powder Inhaler

RxCUI
2166797
RxNorm name
Sensor 200 ACTUAT ProAir 0.09 MG/ACTUAT Dry Powder Inhaler
Display name
Sensor 200 ACTUAT ProAir 0.09 MG/ACTUAT Dry Powder Inhaler
Full name
Sensor 200 ACTUAT ProAir 0.09 MG/ACTUAT Dry Powder Inhaler
Term type
SY
Status
DailyMed mapping
Updated
2026-06-04 23:39:01

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
ProAir DigihalerALBUTEROL SULFATETeva Respiratory, LLC667ce3ec-5217-4b10-b712-f3e54fbbf0872022-06-01Warnings, Adverse reactionsExact identifier
rxcui: 2166797

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
667ce3ec-5217-4b10-b712-f3e54fbbf087ProAir digihaler 90 MCG /INHAL Dry Powder Inhaler, 200 Actuations [PSN] · Sensor 200 ACTUAT albuterol 0.09 MG/ACTUAT Dry Powder Inhaler [ProAir] [SBD] · ProAir digihaler 90 MCG /INHAL Dry Powder Inhaler, 200 Actuations [SY] · Sensor 200 ACTUAT ProAir 0.09 MG/ACTUAT Dry Powder Inhaler [SY]426These highlights do not include all the information needed to use PROAIR DIGIHALER safely and effectively. See full prescribing information for PROAIR DIGIHALER. PROAIR ® DIGIHALER ® (albuterol sulfate) inhalation powder, for oral inhalation use Initial U.S. Approval: 198120220601