FDA.reportPublic FDA data

albuterol 90 MCG /INHAL Dry Powder Inhaler with sensor, 200 Actuations

RxCUI
2166796
RxNorm name
albuterol 90 MCG /INHAL Dry Powder Inhaler with sensor, 200 Actuations
Display name
albuterol 90 MCG /INHAL Dry Powder Inhaler with sensor, 200 Actuations
Full name
albuterol 90 MCG /INHAL Dry Powder Inhaler with sensor, 200 Actuations
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: 2166796

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-f3e54fbbf087albuterol 90 MCG /INHAL Dry Powder Inhaler with sensor, 200 Actuations [PSN] · Sensor 200 ACTUAT albuterol 0.09 MG/ACTUAT Dry Powder Inhaler [SCD] · albuterol 90 MCG /INHAL Dry Powder Inhaler with sensor, 200 Actuations [SY]326These 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