NDC 63629-8294 – Budesonide

Budesonide 3 mg/1 · Capsule, Delayed Release · Oral

Human Prescription Drug

Product NDC63629-8294

Product details

Brand name
Budesonide
Generic name
Budesonide
Labeler
Bryant Ranch Prepack
Dosage form
Capsule, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA206200
Marketed since
September 15, 2017
Listing expires
December 31, 2026
Pharmacologic class
Corticosteroid

Active ingredients

Uses, dosage, side effects and warnings for Budesonide →

Package NDC codes (1)

Package NDCDescriptionSince
63629-8294-130 CAPSULE, DELAYED RELEASE in 1 BOTTLE (63629-8294-1)Feb 6, 2020

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