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Budesonide

NDC 65162-778 · Amneal Pharmaceuticals LLC

Generic nameBudesonide
Dosage formCAPSULE, DELAYED RELEASE
RouteORAL
Active ingredient(s)BUDESONIDE
Strength3 mg/1
Pharmacologic classCorticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
Marketing categoryANDA

Packages

65162-778-10 — 100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (65162-778-10)

65162-778-18 — 180 CAPSULE, DELAYED RELEASE in 1 BOTTLE (65162-778-18)

65162-778-30 — 300 CAPSULE, DELAYED RELEASE in 1 BOTTLE (65162-778-30)

65162-778-49 — 21 CAPSULE, DELAYED RELEASE in 1 BOTTLE (65162-778-49)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

60687-596 — Budesonide, 60687-889 — Budesonide, 61269-509 — Budesonide, 61269-518 — Budesonide, 62135-822 — Budesonide, 62135-823 — Budesonide, 63629-8294 — Budesonide, 64764-105 — Budesonide, 64980-638 — BUDESONIDE, 64980-639 — BUDESONIDE, 65649-651 — budesonide, 68012-309 — budesonide, 68180-984 — budesonide inhalation, 68382-720 — budesonide, 68682-309 — budesonide, 68682-658 — budesonide, 68788-7314 — Budesonide, 68788-8429 — Budesonide, 68788-8503 — budesonide inhalation, 69097-318 — 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.