NDC 0186-1989 – Pulmicort Respules

Budesonide .5 mg/2mL · Suspension · Respiratory (inhalation)

Human Prescription Drug 2 recalls

Product NDC0186-1989

Product details

Brand name
Pulmicort Respules
Generic name
Budesonide
Labeler
AstraZeneca Pharmaceuticals LP
Dosage form
Suspension
Route
Respiratory (inhalation)
Marketing category
NDA · NDA020929
Marketed since
September 8, 2000
Listing expires
December 31, 2026
Pharmacologic class
Corticosteroid

Active ingredients

Uses, dosage, side effects and warnings for Pulmicort Respules →

Package NDC codes (1)

Package NDCDescriptionSince
0186-1989-046 POUCH in 1 CARTON (0186-1989-04) / 5 AMPULE in 1 POUCH / 2 mL in 1 AMPULESep 8, 2000

Recalls mentioning this NDC

Other Pulmicort Respules products