AstraZeneca LP

FDA Regulatory Profile

Summary

Total Recalls
2
510(k) Clearances
0
Inspections
30
Compliance Actions
0

Known Names

astrazeneca, astrazeneca pharmaceuticals, astrazeneca r and d molndal, astrazeneca r and d

Recent Recalls

NumberClassProductDate
D-198-2013Class IIIPULMICORT RESPULES 0.25 mg/2 ml Budesonide Inhalation Suspension (30 ampules/carton) NDC: 0186-1January 11, 2013
D-199-2013Class IIIPULMICORT RESPULES 0.5 mg/2 ml (30 ampules/carton) Budesonide Inhalation Suspension NDC: 0186-1989January 11, 2013