NDC 53746-778 – Budesonide

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

Human Prescription Drug

Product NDC53746-778

Product details

Brand name
Budesonide
Generic name
Budesonide
Labeler
Amneal Pharmaceuticals of New York LLC
Dosage form
Capsule, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA206200
Marketed since
May 22, 2025
Listing expires
December 31, 2026
Pharmacologic class
Corticosteroid

Active ingredients

Uses, dosage, side effects and warnings for Budesonide →

Package NDC codes (1)

Package NDCDescriptionSince
53746-778-10100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (53746-778-10)May 22, 2025

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