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ALBUTEROL SULFATE

NDC 51662-1499 · HF Acquisition Co LLC, DBA HealthFirst

Generic nameALBUTEROL SULFATE
Dosage formSOLUTION
RouteRESPIRATORY (INHALATION)
Active ingredient(s)ALBUTEROL SULFATE
Strength2.5 mg/3mL
Pharmacologic classAdrenergic beta2-Agonists [MoA], beta2-Adrenergic Agonist [EPC]
Marketing categoryANDA

Packages

51662-1499-1 — 5 VIAL, SINGLE-DOSE in 1 POUCH (51662-1499-1) / 3 mL in 1 VIAL, SINGLE-DOSE

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

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, 51407-367 — albuterol sulfate, 51407-368 — albuterol sulfate, 51662-1267 — 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, 59651-183 — ALBUTEROL SULFATE, 59651-184 — ALBUTEROL SULFATE, 59651-333 — 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.