Albuterol

NDC 59651-334 · Aurobindo Pharma Limited

Generic nameAlbuterol

Dosage formTABLET

RouteORAL

Active ingredient(s)ALBUTEROL SULFATE

Strength4 mg/1

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

Marketing categoryANDA

Packages

59651-334-01 — 100 TABLET in 1 BOTTLE (59651-334-01)

59651-334-05 — 500 TABLET in 1 BOTTLE (59651-334-05)

FDA lists these products with the same active ingredient.

51662-1513 — ALBUTEROL SULFATE, 53489-176 — albuterol sulfate, 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, 60429-975 — Ipratropium Bromide and Albuterol Sulfate, 60687-395 — 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, +129 more

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