albuterol sulfate

NDC 51407-367 · Golden State Medical Supply, Inc.

Generic namealbuterol sulfate

Dosage formTABLET

RouteORAL

Active ingredient(s)ALBUTEROL SULFATE

Strength2 mg/1

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

Marketing categoryANDA

Packages

51407-367-01 — 100 TABLET in 1 BOTTLE (51407-367-01)

FDA lists these products with the same active ingredient.

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, 50090-6560 — Albuterol Sulfate, 50742-392 — Albuterol Sulfate, 50742-393 — Albuterol Sulfate, 51407-368 — albuterol sulfate, 51662-1267 — ALBUTEROL SULFATE, 51662-1499 — ALBUTEROL SULFATE, 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, +129 more

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