Ezetimibe and Simvastatin

NDC 43598-742 · Dr.Reddys Laboratories Inc

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

43598-742-10 — 1000 TABLET in 1 BOTTLE (43598-742-10)

43598-742-30 — 30 TABLET in 1 BOTTLE (43598-742-30)

43598-742-90 — 90 TABLET in 1 BOTTLE (43598-742-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

31722-513 — Simvastatin, 31722-514 — Simvastatin, 31722-628 — EZETIMIBE, 33342-373 — Ezetimibe, 42708-148 — simvastatin, 42708-168 — SIMVASTATIN, 42708-169 — SIMVASTATIN, 43063-726 — simvastatin, 43063-727 — simvastatin, 43063-733 — simvastatin, 43598-743 — Ezetimibe and Simvastatin, 43598-744 — Ezetimibe and Simvastatin, 43598-745 — Ezetimibe and Simvastatin, 50090-3422 — Ezetimibe, 50090-3657 — Ezetimibe, 50090-4736 — SIMVASTATIN, 50090-4772 — Ezetimibe and Simvastatin, 50090-4801 — Simvastatin, 50090-4897 — simvastatin, 50090-4901 — 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.