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Albuterol Sulfate

NDC 60687-395 · American Health Packaging

Generic nameAlbuterol Sulfate
Dosage formSOLUTION
RouteRESPIRATORY (INHALATION)
Active ingredient(s)ALBUTEROL SULFATE
Strength2.5 mg/3mL
Pharmacologic classAdrenergic beta2-Agonists [MoA], beta2-Adrenergic Agonist [EPC]
Marketing categoryANDA

Packages

60687-395-83 — 30 POUCH in 1 CARTON (60687-395-83) / 1 AMPULE in 1 POUCH (60687-395-79) / 3 mL in 1 AMPULE

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.

53489-177 — albuterol sulfate, 55154-2132 — Albuterol Sulfate, 55154-4410 — Albuterol Sulfate, 59310-117 — albuterol sulfate, 59310-580 — Albuterol Sulfate, 59651-183 — ALBUTEROL SULFATE, 59651-184 — ALBUTEROL SULFATE, 59651-333 — Albuterol, 59651-334 — Albuterol, 60429-975 — Ipratropium Bromide and Albuterol Sulfate, 60687-405 — Ipratropium Bromide and Albuterol Sulfate, 60687-662 — Albuterol Sulfate, 62135-189 — Albuterol Sulfate, 62135-671 — Albuterol Sulfate, 62135-672 — Albuterol Sulfate, 62135-826 — Albuterol Sulfate, 62135-827 — Albuterol Sulfate, 62135-828 — Albuterol Sulfate, 62135-829 — Albuterol Sulfate, 62135-831 — Ipratropium Bromide and 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.