TOBI Podhaler Daily Kit, 8

RxCUI
1661567
RxNorm name
TOBI Podhaler Daily Kit, 8
Display name
TOBI Podhaler Daily Kit, 8
Full name
TOBI Podhaler Daily Kit, 8
Term type
SY
Status
DailyMed mapping
Updated
2026-06-04 23:39:20

RxNav Current And Historical NDCs#

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UNII Substances#

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openFDA label cross-check#

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Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
TOBI PodhalerTOBRAMYCINViatris Specialty LLCc4b5bb1f-e158-4ac1-9c35-e98a416c743a2026-04-15Warnings, Adverse reactionsExact identifier
rxcui: 1661567

DailyMed RxNorm Mappings#

Set ID, RxNorm string, TTY table
Set IDRxNorm stringTTYSPL versionLabelEffective
c4b5bb1f-e158-4ac1-9c35-e98a416c743aTOBI Podhaler Daily Kit, 8SY12These highlights do not include all the information needed to use TOBI PODHALER safely and effectively. See full prescribing information for TOBI PODHALER. TOBI ® PODHALER ® (tobramycin inhalation powder), for oral inhalation use Initial U.S. Approval: 197520230215
c4b5bb1f-e158-4ac1-9c35-e98a416c743a{8 (tobramycin 28 MG Inhalation Powder [Tobi]) } Pack [TOBI Podhaler Daily Kit]BPCK12These highlights do not include all the information needed to use TOBI PODHALER safely and effectively. See full prescribing information for TOBI PODHALER. TOBI ® PODHALER ® (tobramycin inhalation powder), for oral inhalation use Initial U.S. Approval: 197520230215
c4b5bb1f-e158-4ac1-9c35-e98a416c743aTOBI Podhaler Daily Kit, including 8 capsules (1 Blister Card of 8 Capsules)SY12These highlights do not include all the information needed to use TOBI PODHALER safely and effectively. See full prescribing information for TOBI PODHALER. TOBI ® PODHALER ® (tobramycin inhalation powder), for oral inhalation use Initial U.S. Approval: 197520230215
c4b5bb1f-e158-4ac1-9c35-e98a416c743aTOBI Podhaler 8 Capsule Daily PackPSN12These highlights do not include all the information needed to use TOBI PODHALER safely and effectively. See full prescribing information for TOBI PODHALER. TOBI ® PODHALER ® (tobramycin inhalation powder), for oral inhalation use Initial U.S. Approval: 197520230215