200 ACTUAT albuterol 0.09 MG/ACTUAT Dry Powder Inhaler

RxCUI
1649560
RxNorm name
200 ACTUAT albuterol 0.09 MG/ACTUAT Dry Powder Inhaler
Display name
200 ACTUAT albuterol 0.09 MG/ACTUAT Dry Powder Inhaler
Full name
200 ACTUAT albuterol 0.09 MG/ACTUAT Dry Powder Inhaler
Term type
SCD
Status
DailyMed mapping
Updated
2026-06-04 23:39:08

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
ProAir RespiClickALBUTEROL SULFATETeva Respiratory, LLC9324e2eb-26fd-4f14-9f10-e5aa467306f42022-09-27Warnings, Adverse reactionsExact identifier
rxcui: 1649560

DailyMed RxNorm Mappings#

Set ID, RxNorm string, TTY table
Set IDRxNorm stringTTYSPL versionLabelEffective
9324e2eb-26fd-4f14-9f10-e5aa467306f4albuterol sulfate 90 MCG/INHAL Dry Powder Inhaler, 200 ActuationsPSN11These highlights do not include all the information needed to use PROAIR RESPICLICK safely and effectively. See full prescribing information for PROAIR RESPICLICK. PROAIR® RESPICLICK® (albuterol sulfate) inhalation powder, for oral inhalation use Initial U.S. Approval: 198120220927
9324e2eb-26fd-4f14-9f10-e5aa467306f4albuterol 90 MCG/ACTUAT (albuterol sulfate 108 MCG/ACTUAT from mouthpiece) 200 ACTUAT Dry Powder InhalerSY11These highlights do not include all the information needed to use PROAIR RESPICLICK safely and effectively. See full prescribing information for PROAIR RESPICLICK. PROAIR® RESPICLICK® (albuterol sulfate) inhalation powder, for oral inhalation use Initial U.S. Approval: 198120220927
9324e2eb-26fd-4f14-9f10-e5aa467306f4albuterol 90 MCG/ACTUAT Dry Powder Inhaler, 200 ACTUATSY11These highlights do not include all the information needed to use PROAIR RESPICLICK safely and effectively. See full prescribing information for PROAIR RESPICLICK. PROAIR® RESPICLICK® (albuterol sulfate) inhalation powder, for oral inhalation use Initial U.S. Approval: 198120220927
9324e2eb-26fd-4f14-9f10-e5aa467306f4200 ACTUAT albuterol 0.09 MG/ACTUAT Dry Powder InhalerSCD11These highlights do not include all the information needed to use PROAIR RESPICLICK safely and effectively. See full prescribing information for PROAIR RESPICLICK. PROAIR® RESPICLICK® (albuterol sulfate) inhalation powder, for oral inhalation use Initial U.S. Approval: 198120220927
28e6becd-a65a-4245-b282-5766127567a2200 ACTUAT albuterol 0.09 MG/ACTUAT Dry Powder InhalerSCD5These highlights do not include all the information needed to use PROAIR RESPICLICK safely and effectively. See full prescribing information for PROAIR RESPICLICK. PROAIR® RESPICLICK® (albuterol sulfate) inhalation powder, for oral inhalation use Initial U.S. Approval: 198120230607
28e6becd-a65a-4245-b282-5766127567a2albuterol 90 MCG/ACTUAT Dry Powder Inhaler, 200 ACTUATSY5These highlights do not include all the information needed to use PROAIR RESPICLICK safely and effectively. See full prescribing information for PROAIR RESPICLICK. PROAIR® RESPICLICK® (albuterol sulfate) inhalation powder, for oral inhalation use Initial U.S. Approval: 198120230607
28e6becd-a65a-4245-b282-5766127567a2albuterol sulfate 90 MCG/INHAL Dry Powder Inhaler, 200 ActuationsPSN5These highlights do not include all the information needed to use PROAIR RESPICLICK safely and effectively. See full prescribing information for PROAIR RESPICLICK. PROAIR® RESPICLICK® (albuterol sulfate) inhalation powder, for oral inhalation use Initial U.S. Approval: 198120230607
28e6becd-a65a-4245-b282-5766127567a2albuterol 90 MCG/ACTUAT (albuterol sulfate 108 MCG/ACTUAT from mouthpiece) 200 ACTUAT Dry Powder InhalerSY5These highlights do not include all the information needed to use PROAIR RESPICLICK safely and effectively. See full prescribing information for PROAIR RESPICLICK. PROAIR® RESPICLICK® (albuterol sulfate) inhalation powder, for oral inhalation use Initial U.S. Approval: 198120230607