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ALBUTEROL SULFATE

NDC 72162-2064 · Bryant Ranch Prepack

Generic nameALBUTEROL SULFATE
Dosage formSYRUP
RouteORAL
Active ingredient(s)ALBUTEROL SULFATE
Strength2 mg/5mL
Pharmacologic classAdrenergic beta2-Agonists [MoA], beta2-Adrenergic Agonist [EPC]
Marketing categoryANDA

Packages

72162-2064-2 — 473 mL in 1 BOTTLE (72162-2064-2)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

71205-051 — Ipratropium Bromide and Albuterol Sulfate, 71205-211 — Albuterol Sulfate, 71205-441 — albuterol sulfate, 71205-641 — albuterol sulfate, 71205-726 — Ipratropium Bromide and Albuterol Sulfate, 71205-732 — Albuterol sulfate, 71205-898 — albuterol, 71205-899 — albuterol, 71335-2907 — ALBUTEROL SULFATE, 71872-7054 — Albuterol Sulfate, 75834-273 — albuterol sulfate, 75834-274 — albuterol sulfate, 76204-010 — Albuterol Sulfate, 76204-011 — Albuterol Sulfate, 76204-027 — Albuterol Sulfate, 76204-200 — Albuterol Sulfate, 76204-600 — Ipratropium Bromide and Albuterol Sulfate, 76282-679 — albuterol sulfate, 76420-087 — Albuterol Sulfate, 76420-088 — Albuterol Sulfate, +129 more

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