FDA Drug Recalls

Recalls / Brands / Pulmicort Respules

Pulmicort Respules

2 FDA drug recalls involving brand “Pulmicort Respules.

DateClassProductFirm
2013-01-11Class IIIPULMICORT RESPULES 0.25 mg/2 ml Budesonide Inhalation Suspension (30 ampules/carton) NDC: 0186-1988-04AstraZeneca LP
2013-01-11Class IIIPULMICORT RESPULES 0.5 mg/2 ml (30 ampules/carton) Budesonide Inhalation Suspension NDC: 0186-1989-04AstraZeneca LP