Budesonide

NDC 76282-641 · Exelan Pharmaceuticals, Inc.

Generic nameBudesonide

Dosage formINHALANT

RouteORAL

Active ingredient(s)BUDESONIDE

Strength.5 mg/2mL

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

Marketing categoryANDA

Packages

76282-641-38 — 6 POUCH in 1 CARTON (76282-641-38) / 5 AMPULE in 1 POUCH (76282-641-37) / 2 mL in 1 AMPULE

Billed under HCPCS

J7626 — Budesonide, inhalation solution, fda-approved final product, non-compounded, administered through dme, unit dose form, up to 0.5 mg Medicare Part B payment limit (ASP + 6%): $1.09

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

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, 70771-1075 — budesonide, 72162-2473 — budesonide, 76282-640 — Budesonide, 76282-642 — Budesonide, 81749-004 — budesonide, 85612-010 — Budesonide, 85612-011 — Budesonide, 85766-113 — Budesonide and Formoterol Fumarate Dihydrate, 85766-114 — Budesonide and Formoterol Fumarate Dihydrate, 85766-184 — Budesonide and Formoterol Fumarate Dihydrate, +69 more

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