NDC 0378-4500 – Budesonide

Budesonide 9 mg/1 · Tablet, Film Coated, Extended Release · Oral

Human Prescription Drug

Product NDC0378-4500

Product details

Brand name
Budesonide
Generic name
Budesonide
Labeler
Mylan Pharmaceuticals Inc.
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
ANDA · ANDA208851
Marketed since
October 21, 2020
Listing expires
December 31, 2026
Pharmacologic class
Corticosteroid

Active ingredients

Uses, dosage, side effects and warnings for budesonide →

Package NDC codes (1)

Package NDCDescriptionSince
0378-4500-9330 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0378-4500-93)Oct 21, 2020

Other budesonide products