Ezetimibe

NDC 50090-7339 · A-S Medication Solutions

Generic nameEzetimibe

Dosage formTABLET

RouteORAL

Active ingredient(s)EZETIMIBE

Strength10 mg/1

Pharmacologic classDecreased Cholesterol Absorption [PE], Dietary Cholesterol Absorption Inhibitor [EPC]

Marketing categoryANDA

Packages

50090-7339-0 — 30 TABLET in 1 BOTTLE (50090-7339-0)

50090-7339-1 — 90 TABLET in 1 BOTTLE (50090-7339-1)

FDA lists these products with the same active ingredient.

43598-745 — Ezetimibe and Simvastatin, 50090-3422 — Ezetimibe, 50090-3657 — Ezetimibe, 50090-4772 — Ezetimibe and Simvastatin, 50090-6630 — Ezetimibe, 50090-6631 — Ezetimibe, 50090-7047 — ezetimibe and simvastatin, 50090-7099 — Ezetimibe, 50090-7236 — Ezetimibe, 50090-7338 — Ezetimibe, 50090-7689 — EZETIMIBE, 50090-7690 — EZETIMIBE, 50228-379 — Ezetimibe, 50268-298 — Ezetimibe, 51407-190 — Ezetimibe and Simvastatin, 51407-191 — Ezetimibe and Simvastatin, 51407-192 — Ezetimibe and Simvastatin, 51407-193 — Ezetimibe and Simvastatin, 51660-200 — Ezetimibe, 59651-052 — Ezetimibe, +55 more

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.