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Ezetimibe

NDC 71205-277 · 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

71205-277-30 — 30 TABLET in 1 BOTTLE (71205-277-30)

71205-277-60 — 60 TABLET in 1 BOTTLE (71205-277-60)

71205-277-90 — 90 TABLET in 1 BOTTLE (71205-277-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

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, 70771-1109 — ezetimibe, 71205-145 — 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, +55 more

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