FDA.reportPublic FDA data

budesonide 0.5 MG/ML Inhalation Suspension [Pulmicort]

RxCUI
616819
RxNorm name
budesonide 0.5 MG/ML Inhalation Suspension [Pulmicort]
Display name
budesonide 0.5 MG/ML Inhalation Suspension [Pulmicort]
Full name
budesonide 0.5 MG/ML Inhalation Suspension [Pulmicort]
Term type
SBD
Status
DailyMed mapping
Updated
2026-06-04 23:38:53

RxNav Current And Historical NDCs#

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No records found.

UNII Substances#

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No records found.

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
PULMICORT RESPULESBUDESONIDEAstraZeneca Pharmaceuticals LP33cd9834-76df-4f26-3fa2-aab6b9eee8f22019-10-11Warnings, Adverse reactionsExact identifier
rxcui: 616819

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
33cd9834-76df-4f26-3fa2-aab6b9eee8f2Pulmicort Respules 1 MG in 2 ML Inhalation Suspension [PSN] · budesonide 0.5 MG/ML Inhalation Suspension [Pulmicort] [SBD] · Pulmicort Respules 0.5 MG/ML Inhalation Suspension [SY] · Pulmicort Respules 1 MG per 2 ML Inhalation Suspension [SY]423These highlights do not include all the information needed to use PULMICORT RESPULES ® safely and effectively. See full prescribing information for PULMICORT RESPULES ® . PULMICORT RESPULES ® (budesonide) inhalation suspension Initial U.S. Approval: 200020191011