Ezetimibe

NDC 76333-170 · Orient Pharma Co., Ltd.

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

76333-170-12 — 1000 TABLET in 1 BOTTLE (76333-170-12)

76333-170-13 — 500 TABLET in 1 BOTTLE (76333-170-13)

76333-170-14 — 90 TABLET in 1 BOTTLE (76333-170-14)

76333-170-15 — 30 TABLET in 1 BOTTLE (76333-170-15)

FDA lists these products with the same active ingredient.

69238-1156 — Ezetimibe and Simvastatin, 69238-1157 — Ezetimibe and Simvastatin, 69238-1158 — Ezetimibe and Simvastatin, 70771-1109 — ezetimibe, 71205-145 — Ezetimibe, 71205-277 — Ezetimibe, 71335-0684 — Ezetimibe, 71335-0933 — Ezetimibe, 71335-1127 — Ezetimibe, 71335-2123 — Ezetimibe, 71335-3092 — EZETIMIBE, 72426-818 — Bempedoic Acid and Ezetimibe, 78206-174 — ezetimibe and simvastatin, 78206-175 — ezetimibe and simvastatin, 78206-176 — ezetimibe and simvastatin, 78206-177 — ezetimibe and simvastatin, 78206-178 — Ezetimibe, 82009-024 — ezetimibe, 82804-064 — Ezetimibe, 82804-211 — 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.