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PULMICORT RESPULES

NDC 0186-1989 · AstraZeneca Pharmaceuticals LP

Generic nameBudesonide
Dosage formSUSPENSION
RouteRESPIRATORY (INHALATION)
Active ingredient(s)BUDESONIDE
Strength.5 mg/2mL
Pharmacologic classCorticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
Marketing categoryNDA

Packages

0186-1989-04 — 6 POUCH in 1 CARTON (0186-1989-04) / 5 AMPULE in 1 POUCH / 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.

0093-6815 — Budesonide, 0093-6816 — Budesonide, 0093-6817 — Budesonide, 0115-1687 — Budesonide, 0115-1689 — Budesonide, 0186-0370 — Budesonide and Formoterol Fumarate Dihydrate, 0186-0372 — Budesonide and Formoterol Fumarate Dihydrate, 0186-1988 — Budesonide, 0186-1990 — Budesonide, 0310-4616 — budesonide, glycopyrrolate, and formoterol fumarate, 0310-6616 — budesonide, glycopyrrolate, and formoterol fumarate, 0310-7370 — Budesonide and Formoterol Fumarate Dihydrate, 0310-7372 — Budesonide and Formoterol Fumarate Dihydrate, 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, +69 more

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