Skip to main content

Ezetimibe

NDC 82804-064 · Proficient Rx LP

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

82804-064-30 — 30 TABLET in 1 BOTTLE (82804-064-30)

82804-064-60 — 60 TABLET in 1 BOTTLE (82804-064-60)

82804-064-90 — 90 TABLET in 1 BOTTLE (82804-064-90)

Related Codes

Same active ingredient

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, 82009-024 — 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.