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Albuterol

NDC 69238-1345 · Amneal Pharmaceuticals NY LLC

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

69238-1345-1 — 100 TABLET in 1 BOTTLE (69238-1345-1)

69238-1345-5 — 500 TABLET in 1 BOTTLE (69238-1345-5)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

68788-8787 — Albuterol Sulfate, 68788-8874 — Albuterol Sulfate, 68788-8878 — Albuterol sulfate, 68999-189 — Albuterol Sulfate, 69097-021 — Albuterol Sulfate, 69097-142 — albuterol sulfate, 69097-173 — Ipratropium Bromide and Albuterol Sulfate, 69097-840 — Ipratropium Bromide and Albuterol Sulfate, 69238-1291 — Albuterol Sulfate, 69238-1344 — Albuterol, 70518-1081 — albuterol sulfate, 70518-1237 — albuterol sulfate, 70518-2072 — albuterol sulfate, 70518-3541 — Albuterol sulfate, 70518-3560 — albuterol sulfate, 70518-4490 — ALBUTEROL SULFATE, 70518-4496 — Albuterol Sulfate, 70518-4528 — Albuterol Sulfate, 70710-1061 — Albuterol, 70710-1062 — Albuterol, +129 more

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