ezetimibe

NDC 70771-1109 · Zydus Lifesciences Limited

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

70771-1109-0 — 1000 TABLET in 1 BOTTLE (70771-1109-0)

70771-1109-1 — 100 TABLET in 1 BOTTLE (70771-1109-1)

70771-1109-3 — 30 TABLET in 1 BOTTLE (70771-1109-3)

70771-1109-4 — 10 BLISTER PACK in 1 CARTON (70771-1109-4) / 10 TABLET in 1 BLISTER PACK (70771-1109-2)

70771-1109-5 — 500 TABLET in 1 BOTTLE (70771-1109-5)

70771-1109-9 — 90 TABLET in 1 BOTTLE (70771-1109-9)

FDA lists these products with the same active ingredient.

68462-226 — Ezetimibe, 68462-321 — ezetimibe and simvastatin, 68462-322 — ezetimibe and simvastatin, 68462-323 — ezetimibe and simvastatin, 68462-324 — ezetimibe and simvastatin, 69238-1154 — Ezetimibe, 69238-1155 — Ezetimibe and Simvastatin, 69238-1156 — Ezetimibe and Simvastatin, 69238-1157 — Ezetimibe and Simvastatin, 69238-1158 — Ezetimibe and Simvastatin, 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, 76333-170 — Ezetimibe, 78206-174 — 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.