Class II · Moderate risk
Pulmicort Respules 0.5 mg/2mL s
Lack of Processing Controls.
National Drug Code
Is NDC 0186-1989-04 recalled?
Pulmicort Respules · 6 POUCH in 1 CARTON (0186-1989-04) / 5 AMPULE in 1 POUCH / 2 mL in 1 AMPULE
Yes — this exact package was recalled
2 FDA recalls name the code 0186-1989-04 directly. A recall still applies to particular lot numbers — compare the lot on your package with the FDA notice below, and talk to your pharmacist before stopping a prescribed medication.
- Active ingredient
- Budesonide
- Strength
- BUDESONIDE .5 mg/2mL
- Form
- Suspension · Respiratory (inhalation)
- Labeler
- AstraZeneca Pharmaceuticals LP
- Type
- Human Prescription Drug
- Product code
- 0186-1989
Recalls naming this package
Class III · Low risk
PULMICORT RESPULES 0.5 mg/2 ml
Does Not Meet Monograph: Budesonide may be slightly above or below the specification range.
Where to find this code. The NDC is printed on the pharmacy label and on the manufacturer's carton, usually as three groups of digits after “NDC”. The last group is the package size — two bottles of the same medicine can differ only in that group, and a recall may cover one but not the other.
Other recalled products from this labeler
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