Skip to main content
MedicHelpLine
Join Free
Verified Professional Network190+ CountriesHIPAA-Aware Platform
Back to Drug Index
General MedicationsINHALATIONGeneric

PULMICORT

BUDESONIDE

Standard Dose
0.32MG/INH
Max Dose
Refer to approved labeling
Primary Use
Review priority: STANDARD Marketing status: Discontinued
Summary

Approval overview PULMICORT is listed in Drugs@FDA under application 020441 (NDA).

Review priority: STANDARD Marketing status: Discontinued Active ingredient BUDESONIDE Form and strength POWDER, METERED;INHALATION - 0.32MG/INH Sponsor ASTRAZENECA Submission history Latest submission status date: 2007-08-20 00:00:00.

Structured Monograph

Clinical summary

Approval overview PULMICORT is listed in Drugs@FDA under application 020441 (NDA). Review priority: STANDARD Marketing status: Discontinued Active ingredient BUDESONIDE Form and strength POWDER, METERED;INHALATION - 0.32MG/INH Sponsor ASTRAZENECA Submission history Latest submission status date: 2007-08-20 00:00:00. Submission type: SUPPL.

Monitoring

  • • Marketing status: Discontinued
  • • Review priority: STANDARD

Interaction Notes

  • No interaction notes stored yet.