AstraZeneca LP recalls PULMICORT RESPULES 0.25 mg/2 ml Budesonide Inhalation Susp
Recalled Product
PULMICORT RESPULES 0.25 mg/2 ml Budesonide Inhalation Suspension (30 ampules/carton) NDC: 0186-1988-04
Hazard / Issue
Does Not Meet Monograph: Budesonide may be slightly above or below the specification range.
Issued by
FDA
Distribution: Nationwide (United States)
Lot/Code Info: Lot/Exp date: AH0054 Exp 5/14; AK0125 Exp 7/14
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