budesonide

NDC 68382-720 · Zydus Pharmaceuticals USA Inc.

Generic namebudesonide

Dosage formCAPSULE, COATED PELLETS

RouteORAL

Active ingredient(s)BUDESONIDE

Strength3 mg/1

Pharmacologic classCorticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]

Marketing categoryANDA

Packages

68382-720-01 — 100 CAPSULE, COATED PELLETS in 1 BOTTLE (68382-720-01)

68382-720-05 — 500 CAPSULE, COATED PELLETS in 1 BOTTLE (68382-720-05)

68382-720-06 — 30 CAPSULE, COATED PELLETS in 1 BOTTLE (68382-720-06)

68382-720-10 — 1000 CAPSULE, COATED PELLETS in 1 BOTTLE (68382-720-10)

68382-720-16 — 90 CAPSULE, COATED PELLETS in 1 BOTTLE (68382-720-16)

68382-720-77 — 10 BLISTER PACK in 1 CARTON (68382-720-77) / 10 CAPSULE, COATED PELLETS in 1 BLISTER PACK (68382-720-30)

FDA lists these products with the same active ingredient.

62135-822 — Budesonide, 62135-823 — Budesonide, 63629-8294 — Budesonide, 64764-105 — Budesonide, 64980-638 — BUDESONIDE, 64980-639 — BUDESONIDE, 65162-778 — Budesonide, 65649-651 — budesonide, 68012-309 — budesonide, 68180-984 — budesonide inhalation, 68682-309 — budesonide, 68682-658 — budesonide, 68788-7314 — Budesonide, 68788-8429 — Budesonide, 68788-8503 — budesonide inhalation, 69097-318 — Budesonide, 69097-319 — Budesonide, 69097-321 — Budesonide, 69842-001 — Budesonide, 70518-4613 — budesonide, +69 more

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.