NDC 65162-778 – Budesonide

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

Human Prescription Drug

Product NDC65162-778

Product details

Brand name
Budesonide
Generic name
Budesonide
Labeler
Amneal Pharmaceuticals LLC
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 (4)

Package NDCDescriptionSince
65162-778-10100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (65162-778-10)Sep 15, 2017
65162-778-18180 CAPSULE, DELAYED RELEASE in 1 BOTTLE (65162-778-18)Sep 15, 2017
65162-778-30300 CAPSULE, DELAYED RELEASE in 1 BOTTLE (65162-778-30)Sep 15, 2017
65162-778-4921 CAPSULE, DELAYED RELEASE in 1 BOTTLE (65162-778-49)Sep 15, 2017

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