Albuterol Sulfate

NDC 47335-703 · Sun Pharmaceutical Industries, Inc.

Generic namealbuterol sulfate

Dosage formSOLUTION

RouteRESPIRATORY (INHALATION)

Active ingredient(s)ALBUTEROL SULFATE

Strength.83 mg/mL

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

Marketing categoryANDA

Packages

47335-703-49 — 5 POUCH in 1 CARTON (47335-703-49) / 5 VIAL in 1 POUCH / 3 mL in 1 VIAL

47335-703-52 — 6 POUCH in 1 CARTON (47335-703-52) / 5 VIAL in 1 POUCH / 3 mL in 1 VIAL

47335-703-54 — 12 POUCH in 1 CARTON (47335-703-54) / 5 VIAL in 1 POUCH / 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.

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, 47335-756 — Ipratropium Bromide and Albuterol Sulfate, 50090-0516 — Albuterol Sulfate, 50090-1158 — albuterol sulfate, 50090-1159 — albuterol sulfate, 50090-1382 — Ipratropium Bromide and Albuterol Sulfate, 50090-1669 — Ipratropium Bromide and Albuterol Sulfate, 50090-4137 — albuterol sulfate, 50090-5179 — albuterol sulfate, 50090-5231 — Albuterol sulfate, 50090-5735 — 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.