Budesonide

NDC 47335-633 · Sun Pharmaceutical Industries, Inc.

Generic nameBudesonide

Dosage formSUSPENSION

RouteRESPIRATORY (INHALATION)

Active ingredient(s)BUDESONIDE

Strength1 mg/2mL

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

Marketing categoryANDA

Packages

47335-633-49 — 6 POUCH in 1 CARTON (47335-633-49) / 5 AMPULE in 1 POUCH (47335-633-48) / 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.

0487-9701 — BUDESONIDE, 0536-1112 — Budesonide, 0536-1456 — Budesonide, 0574-9855 — budesonide, 0591-2510 — Budesonide, 0904-7313 — budesonide, 16714-829 — budesonide, 45802-627 — budesonide, 47335-631 — Budesonide, 47335-632 — Budesonide, 49035-703 — Budesonide, 50090-1403 — Budesonide and Formoterol Fumarate Dihydrate, 50090-1467 — Budesonide, 50090-2239 — Budesonide, 50090-4508 — Budesonide and Formoterol Fumarate Dihydrate, 50090-4509 — Budesonide and Formoterol Fumarate Dihydrate, 50090-4510 — Budesonide and Formoterol Fumarate Dihydrate, 50090-6327 — Budesonide and Formoterol Fumarate Dihydrate, 50090-6382 — Budesonide and Formoterol Fumarate Dihydrate, 50090-6586 — Budesonide, +69 more

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