PULMICORT RESPULES 0.25 mg/2 ml Budesonide Inhalation Suspension (30 ampules/carton) NDC: 0186-1988-04
Recall Number: D-198-2013
Firm: AstraZeneca LP
Classification: Class III
Status: Terminated
Report Date: 20130320
Initiation Date: 20130111
Termination Date: 20130726
Reason for Recall
Does Not Meet Monograph: Budesonide may be slightly above or below the specification range.
Product Description
PULMICORT RESPULES 0.25 mg/2 ml Budesonide Inhalation Suspension (30 ampules/carton) NDC: 0186-1988-04