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Albuterol Sulfate

NDC 68071-4754 · NuCare Pharmaceuticals,Inc.

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

68071-4754-2 — 3 mL in 1 VIAL, SINGLE-DOSE (68071-4754-2)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

65862-858 — ALBUTEROL SULFATE, 65862-906 — Ipratropium Bromide and Albuterol Sulfate, 66993-019 — albuterol sulfate, 67296-2315 — Ipratropium Bromide and Albuterol Sulfate, 68071-1670 — albuterol sulfate, 68071-1890 — albuterol sulfate, 68071-2300 — Albuterol sulfate, 68071-3780 — Albuterol Sulfate, 68071-3902 — Albuterol Sulfate, 68071-4543 — Albuterol Sulfate, 68071-4777 — albuterol sulfate, 68071-4940 — Albuterol Sulfate, 68071-5312 — Albuterol Sulfate, 68084-949 — Albuterol Sulfate, 68180-963 — Albuterol sulfate, 68788-4041 — Albuterol Sulfate, 68788-7573 — ALBUTEROL SULFATE, 68788-7996 — Albuterol Sulfate, 68788-8103 — Ipratropium Bromide and Albuterol Sulfate, 68788-8399 — 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.