NDC 60687-889 – Budesonide

Budesonide .25 mg/2mL · Suspension · Respiratory (inhalation)

Human Prescription Drug

Product NDC60687-889

Product details

Brand name
Budesonide
Generic name
Budesonide
Labeler
American Health Packaging
Dosage form
Suspension
Route
Respiratory (inhalation)
Marketing category
ANDA · ANDA211922
Marketed since
May 15, 2026
Listing expires
December 31, 2027
Pharmacologic class
Corticosteroid

Active ingredients

Uses, dosage, side effects and warnings for Budesonide →

Package NDC codes (1)

Package NDCDescriptionSince
60687-889-8330 POUCH in 1 CARTON (60687-889-83) / 1 AMPULE in 1 POUCH (60687-889-79) / 2 mL in 1 AMPULEMay 15, 2026

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