ezetimibe

NDC 68382-773 · Zydus Pharmaceuticals USA 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

68382-773-01 — 100 TABLET in 1 BOTTLE (68382-773-01)

68382-773-05 — 500 TABLET in 1 BOTTLE (68382-773-05)

68382-773-06 — 30 TABLET in 1 BOTTLE (68382-773-06)

68382-773-10 — 1000 TABLET in 1 BOTTLE (68382-773-10)

68382-773-16 — 90 TABLET in 1 BOTTLE (68382-773-16)

68382-773-77 — 10 BLISTER PACK in 1 CARTON (68382-773-77) / 10 TABLET in 1 BLISTER PACK (68382-773-30)

FDA lists these products with the same active ingredient.

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, 67877-508 — Ezetimibe and Simvastatin, 67877-509 — Ezetimibe and Simvastatin, 67877-510 — Ezetimibe and Simvastatin, 68462-226 — Ezetimibe, 68462-321 — ezetimibe and simvastatin, 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, +55 more

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.