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Albuterol Sulfate

NDC 70518-3560 · REMEDYREPACK INC.

Generic namealbuterol sulfate
Dosage formSOLUTION
RouteRESPIRATORY (INHALATION)
Active ingredient(s)ALBUTEROL SULFATE
Strength.83 mg/mL
Pharmacologic classAdrenergic beta2-Agonists [MoA], beta2-Adrenergic Agonist [EPC]
Marketing categoryANDA

Packages

70518-3560-1 — 5 POUCH in 1 CARTON (70518-3560-1) / 5 VIAL in 1 POUCH / 3 mL in 1 VIAL

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

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, 69238-1345 — Albuterol, 70518-1081 — albuterol sulfate, 70518-1237 — albuterol sulfate, 70518-2072 — albuterol sulfate, 70518-3541 — Albuterol sulfate, 70518-4490 — ALBUTEROL SULFATE, 70518-4496 — Albuterol Sulfate, 70518-4528 — Albuterol Sulfate, 70710-1061 — Albuterol, 70710-1062 — Albuterol, 70752-102 — ALBUTEROL SULFATE, 70771-1511 — Albuterol, 70771-1512 — Albuterol, 71205-051 — Ipratropium Bromide and Albuterol Sulfate, 71205-211 — 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.