NDC 68382-720 – budesonide

Budesonide 3 mg/1 · Capsule, Coated Pellets · Oral

Human Prescription Drug

Product NDC68382-720

Product details

Brand name
budesonide
Generic name
budesonide
Labeler
Zydus Pharmaceuticals USA Inc.
Dosage form
Capsule, Coated Pellets
Route
Oral
Marketing category
ANDA · ANDA206134
Marketed since
June 8, 2017
Listing expires
December 31, 2026
Pharmacologic class
Corticosteroid

Active ingredients

Uses, dosage, side effects and warnings for budesonide →

Package NDC codes (6)

Package NDCDescriptionSince
68382-720-01100 CAPSULE, COATED PELLETS in 1 BOTTLE (68382-720-01)Jun 8, 2017
68382-720-05500 CAPSULE, COATED PELLETS in 1 BOTTLE (68382-720-05)Jun 8, 2017
68382-720-0630 CAPSULE, COATED PELLETS in 1 BOTTLE (68382-720-06)Jun 8, 2017
68382-720-101000 CAPSULE, COATED PELLETS in 1 BOTTLE (68382-720-10)Jun 8, 2017
68382-720-1690 CAPSULE, COATED PELLETS in 1 BOTTLE (68382-720-16)Jun 8, 2017
68382-720-7710 BLISTER PACK in 1 CARTON (68382-720-77) / 10 CAPSULE, COATED PELLETS in 1 BLISTER PACK (68382-720-30)Jun 8, 2017

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