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Ezetimibe

NDC 51660-200 · Ohm Laboratories Inc.

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

51660-200-05 — 500 TABLET in 1 BOTTLE (51660-200-05)

51660-200-30 — 30 TABLET in 1 BOTTLE (51660-200-30)

51660-200-90 — 90 TABLET in 1 BOTTLE (51660-200-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

50090-7338 — Ezetimibe, 50090-7339 — Ezetimibe, 50090-7689 — EZETIMIBE, 50090-7690 — EZETIMIBE, 50228-379 — Ezetimibe, 50268-298 — Ezetimibe, 51407-190 — Ezetimibe and Simvastatin, 51407-191 — Ezetimibe and Simvastatin, 51407-192 — Ezetimibe and Simvastatin, 51407-193 — Ezetimibe and Simvastatin, 59651-052 — Ezetimibe, 59651-835 — Ezetimibe and Simvastatin, 59651-836 — Ezetimibe and Simvastatin, 59651-837 — Ezetimibe and Simvastatin, 59651-838 — Ezetimibe and Simvastatin, 60429-982 — Ezetimibe, 60687-373 — Ezetimibe, 63629-7413 — Ezetimibe, 67877-490 — Ezetimibe, 67877-507 — 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.