Albuterol

NDC 0378-7058 · Mylan Pharmaceuticals Inc.

Generic nameAlbuterol

Dosage formSOLUTION

RouteRESPIRATORY (INHALATION)

Active ingredient(s)ALBUTEROL SULFATE

Strength1.25 mg/3mL

Pharmacologic classAdrenergic beta2-Agonists [MoA], beta2-Adrenergic Agonist [EPC]

Marketing categoryANDA

Packages

0378-7058-52 — 5 POUCH in 1 CARTON (0378-7058-52) / 5 VIAL in 1 POUCH (0378-7058-98) / 3 mL in 1 VIAL

Billed under HCPCS

J7613 — Albuterol, inhalation solution, fda-approved final product, non-compounded, administered through dme, unit dose, 1 mg Medicare Part B payment limit (ASP + 6%): $0.06

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0054-0742 — Albuterol Sulfate, 0093-3174 — Albuterol Sulfate, 0173-0682 — albuterol sulfate, 0310-9080 — Albuterol sulfate and budesonide, 0378-7057 — Albuterol, 0378-8270 — Albuterol Sulfate, 0378-9671 — Ipratropium Bromide and Albuterol Sulfate, 0487-0201 — Ipratropium Bromide and Albuterol Sulfate, 0487-0301 — Albuterol Sulfate, 0487-9501 — Albuterol Sulfate, 0487-9901 — Albuterol Sulfate, 0487-9904 — Albuterol Sulfate, 0597-0024 — ipratropium bromide and albuterol, 0781-7296 — Albuterol Sulfate, 17270-0740 — Albuterol Sulfate, 45802-088 — albuterol sulfate, 47335-703 — albuterol sulfate, 47335-756 — Ipratropium Bromide and Albuterol Sulfate, 50090-0516 — Albuterol Sulfate, 50090-1158 — albuterol sulfate, +129 more

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