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Ezetimibe

NDC 63629-7413 · Bryant Ranch Prepack

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

63629-7413-1 — 30 TABLET in 1 BOTTLE (63629-7413-1)

63629-7413-2 — 90 TABLET in 1 BOTTLE (63629-7413-2)

63629-7413-3 — 28 TABLET in 1 BOTTLE (63629-7413-3)

63629-7413-4 — 18 TABLET in 1 BOTTLE (63629-7413-4)

63629-7413-5 — 60 TABLET in 1 BOTTLE (63629-7413-5)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

51407-192 — Ezetimibe and Simvastatin, 51407-193 — Ezetimibe and Simvastatin, 51660-200 — Ezetimibe, 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, 67877-490 — Ezetimibe, 67877-507 — Ezetimibe and Simvastatin, 67877-508 — Ezetimibe and Simvastatin, 67877-509 — Ezetimibe and Simvastatin, 67877-510 — Ezetimibe and Simvastatin, 68382-773 — ezetimibe, 68462-226 — Ezetimibe, 68462-321 — ezetimibe and simvastatin, 68462-322 — ezetimibe and simvastatin, 68462-323 — 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.