EZETIMIBE

NDC 16729-433 · Accord Healthcare Inc.

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

16729-433-10 — 30 TABLET in 1 BOTTLE (16729-433-10)

FDA lists these products with the same active ingredient.

0781-5690 — Ezetimibe, 0904-7103 — Ezetimibe, 10135-787 — Ezetimibe, 16714-778 — ezetimibe and simvastatin, 16714-779 — ezetimibe and simvastatin, 16714-780 — ezetimibe and simvastatin, 16714-781 — ezetimibe and simvastatin, 16714-813 — 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, 50090-3657 — Ezetimibe, 50090-4772 — Ezetimibe and Simvastatin, 50090-6630 — Ezetimibe, 50090-6631 — Ezetimibe, 50090-7047 — ezetimibe and simvastatin, +55 more

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