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ezetimibe and simvastatin

NDC 68462-321 · Glenmark Pharmaceuticals Inc., USA

Generic nameezetimibe and simvastatin
Dosage formTABLET
RouteORAL
Active ingredient(s)EZETIMIBE, SIMVASTATIN
Strength10; 10 mg/1; mg/1
Pharmacologic classDecreased Cholesterol Absorption [PE], Dietary Cholesterol Absorption Inhibitor [EPC], HMG-CoA Reductase Inhibitor [EPC], Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]
Marketing categoryANDA

Packages

68462-321-10 — 1000 TABLET in 1 BOTTLE (68462-321-10)

68462-321-30 — 30 TABLET in 1 BOTTLE (68462-321-30)

68462-321-90 — 90 TABLET in 1 BOTTLE (68462-321-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

68071-4998 — simvastatin, 68084-511 — Simvastatin, 68084-512 — Simvastatin, 68180-464 — SIMVASTATIN, 68180-465 — SIMVASTATIN, 68180-478 — SIMVASTATIN, 68180-479 — SIMVASTATIN, 68180-482 — SIMVASTATIN, 68382-773 — ezetimibe, 68462-226 — Ezetimibe, 68462-322 — ezetimibe and simvastatin, 68462-323 — ezetimibe and simvastatin, 68462-324 — ezetimibe and simvastatin, 68788-8342 — SIMVASTATIN, 68788-8369 — SIMVASTATIN, 68788-8406 — SIMVASTATIN, 69238-1154 — Ezetimibe, 69238-1155 — Ezetimibe and Simvastatin, 69238-1156 — Ezetimibe and Simvastatin, 69238-1157 — Ezetimibe and Simvastatin, +214 more

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