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Albuterol

NDC 64980-443 · Rising Pharma Holdings, Inc.

Generic namealbuterol
Dosage formTABLET
RouteORAL
Active ingredient(s)ALBUTEROL SULFATE
Strength4 mg/1
Pharmacologic classAdrenergic beta2-Agonists [MoA], beta2-Adrenergic Agonist [EPC]
Marketing categoryANDA

Packages

64980-443-01 — 100 TABLET in 1 BOTTLE (64980-443-01)

64980-443-50 — 500 TABLET in 1 BOTTLE (64980-443-50)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

62135-672 — Albuterol Sulfate, 62135-826 — Albuterol Sulfate, 62135-827 — Albuterol Sulfate, 62135-828 — Albuterol Sulfate, 62135-829 — Albuterol Sulfate, 62135-831 — Ipratropium Bromide and Albuterol Sulfate, 63187-026 — albuterol sulfate, 63187-204 — Albuterol Sulfate, 63629-2611 — albuterol, 64980-442 — albuterol, 64980-641 — Albuterol Sulfate, 64980-642 — Albuterol Sulfate, 64980-643 — Albuterol Sulfate, 64980-644 — Albuterol Sulfate, 64980-645 — Ipratropium Bromide and Albuterol Sulfate, 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, +129 more

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