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ALBUTEROL SULFATE

NDC 70752-102 · QUAGEN PHARMACEUTICALS LLC

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

70752-102-12 — 473 mL in 1 BOTTLE (70752-102-12)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

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, 70771-1511 — Albuterol, 70771-1512 — Albuterol, 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, +129 more

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