ezetimibe

NDC 82009-024 · Quallent Pharmaceuticals Health LLC

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

82009-024-05 — 500 TABLET in 1 BOTTLE (82009-024-05)

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, 76333-170 — Ezetimibe, 78206-174 — ezetimibe and simvastatin, 78206-175 — ezetimibe and simvastatin, 78206-176 — ezetimibe and simvastatin, 78206-177 — ezetimibe and simvastatin, 78206-178 — Ezetimibe, 82804-064 — Ezetimibe, 82804-211 — 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.