NDC 0093-6817 – Budesonide

Budesonide 1 mg/2mL · Suspension · Respiratory (inhalation)

Human Prescription Drug

Product NDC0093-6817

Product details

Brand name
Budesonide
Generic name
Budesonide
Labeler
Teva Pharmaceuticals USA, Inc.
Dosage form
Suspension
Route
Respiratory (inhalation)
Marketing category
ANDA · ANDA204548
Marketed since
March 11, 2016
Listing expires
December 31, 2026
Pharmacologic class
Corticosteroid

Active ingredients

Uses, dosage, side effects and warnings for Budesonide →

Package NDC codes (1)

Package NDCDescriptionSince
0093-6817-736 POUCH in 1 CARTON (0093-6817-73) / 5 AMPULE in 1 POUCH (0093-6817-45) / 2 mL in 1 AMPULE (0093-6817-19)Mar 11, 2016

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