Budesonide

NDC 0536-1456 · Rugby Laboratories

Generic nameBudesonide

Dosage formSPRAY, METERED

RouteNASAL

Active ingredient(s)BUDESONIDE

Strength32 ug/1

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

Marketing categoryANDA

Packages

0536-1456-84 — 1 BOTTLE, SPRAY in 1 CARTON (0536-1456-84) / 120 SPRAY, METERED in 1 BOTTLE, SPRAY

FDA lists these products with the same active ingredient.

0310-9080 — Albuterol sulfate and budesonide, 0363-0048 — Budesonide, 0378-4500 — Budesonide, 0378-7502 — Budesonide and Formoterol Fumarate, 0378-7503 — Budesonide and Formoterol Fumarate, 0480-3080 — Budesonide and formoterol fumarate dihydrate, 0480-3081 — Budesonide and formoterol fumarate dihydrate, 0487-9601 — BUDESONIDE, 0487-9701 — BUDESONIDE, 0536-1112 — Budesonide, 0574-9855 — budesonide, 0591-2510 — Budesonide, 0904-7313 — budesonide, 16714-829 — budesonide, 45802-627 — budesonide, 47335-631 — Budesonide, 47335-632 — Budesonide, 47335-633 — Budesonide, 49035-703 — Budesonide, 50090-1403 — 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.