Ezetimibe

NDC 50090-3657 · 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

50090-3657-0 — 30 TABLET in 1 BOTTLE, PLASTIC (50090-3657-0)

50090-3657-1 — 90 TABLET in 1 BOTTLE (50090-3657-1)

FDA lists these products with the same active ingredient.

16714-781 — ezetimibe and simvastatin, 16714-813 — Ezetimibe, 16729-433 — EZETIMIBE, 31722-628 — EZETIMIBE, 33342-373 — Ezetimibe, 43598-742 — Ezetimibe and Simvastatin, 43598-743 — Ezetimibe and Simvastatin, 43598-744 — Ezetimibe and Simvastatin, 43598-745 — Ezetimibe and Simvastatin, 50090-3422 — 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, 50090-7339 — Ezetimibe, 50090-7689 — EZETIMIBE, 50090-7690 — EZETIMIBE, +55 more

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