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ezetimibe 10 MG Simvastatin 20 MG Oral Tablet

1 INDICATIONS AND USAGE Therapy with lipid-altering agents should be only one component of multiple risk factor intervention in individuals at significantly increased risk for atherosclerotic vascular disease due to hypercholesterolemia. Drug therapy is indicated as an adjunct to diet when the response to a diet restricted in saturated fat and cholesterol and other nonpharmacologic measures alone has been inadequate. Ezetimibe and simvastatin tablets, which contain a cholesterol absorption inhibitor and an HMG-CoA reductase inhibitor (statin), are indicated as adjunctive therapy to diet to: • reduce elevated total-C, LDL-C, Apo B, TG, and non-HDL-C, and to increase HDL-C in patients with primary (heterozygous familial and non-familial) hyperlipidemia or mixed hyperlipidemia. ( 1.1 ) • reduce elevated total-C and LDL-C in patients with homozygous familial hypercholesterolemia (HoFH), as an adjunct to other lipid-lowering treatments. ( 1.2 ) Limitations of Use ( 1.3 ) • No incremental benefit of ezetimibe and simvastatin tablets on cardiovascular morbidity and mortality over and above that demonstrated for simvastatin has been established. • Ezetimibe and simvastatin tablets have not been studied in Fredrickson Type I, III, IV, and V dyslipidemias. 1.1 Primary hyperlipidemia Ezetimibe and simvastatin tablets are indicated for the reduction of elevated total cholesterol (total-C), low-density lipoprotein cholesterol (LDL-C), apolipoprotein B (Apo B), triglycerides (TG), and non-high-density lipoprotein cholesterol (non-HDL-C), and to increase high-density lipoprotein cholesterol (HDL-C) in patients with primary (heterozygous familial and non-familial) hyperlipidemia or mixed hyperlipidemia. 1.2 Homozygous Familial hypercholesterolemia (HoFH) Ezetimibe and simvastatin tablets are indicated for the reduction of elevated total-C and LDL-C in patients with homozygous familial hypercholesterolemia, as an adjunct to other lipid-lowering treatments (e.g., LDL apheresis) or if such treatments are unavailable. 1.3 Limitations of Use No incremental benefit of ezetimibe and simvastatin tablets on cardiovascular morbidity and mortality over and above that demonstrated for simvastatin has been established. Ezetimibe and simvastatin tablets have not been studied in Fredrickson type I, III, IV, and V dyslipidemias.

dr.reddys laboratories inc


4 years ago OVAL WHITE Teva 7585 ezetimibe 10 MG  Simvastatin 20 MG Oral Tablet

OVAL WHITE Teva 7585

16 HOW SUPPLIED/STORAGE AND HANDLING

EZETIMIBE AND SIMVASTATIN tablets are available as follows: 10 mg/10 mg- white to off-white, capsule-shaped tablets, debossed with "DRL" on one side of the tablet and with "583" on the other side. They contain 10 mg of ezetimibe and 10 mg of simvastatin. They are available in : Bottles of 30 NDC 43598-742-30 Bottles of 90 NDC 43598-742-90 Bottles of 1000 NDC 43598-742-10 10 mg/20 mg- white to off-white, capsule-shaped tablets, debossed with "DRL" on one side of the tablet and with "584" on the other side. They contain 10 mg of ezetimibe and 20 mg of simvastatin. They are available in : Bottles of 30 NDC 43598-744-30 Bottles of 90 NDC 43598-744-90 Bottles of 1000 NDC 43598-744-10 10 mg/40 mg- white to off-white, capsule-shaped tablets, debossed with "DRL" on one side of the tablet and with "585" on the other side. They contain 10 mg of ezetimibe and 40 mg of simvastatin. They are available in : Bottles of 30 NDC 43598-743-30 Bottles of 90 NDC 43598-743-90 Bottles of 500 NDC 43598-743-05 10 mg/80 mg- white to off-white, capsule-shaped tablets, debossed with "DRL" on one side of the tablet and with "586" on the other side. They contain 10 mg of ezetimibe and 80 mg of simvastatin. They are available in : Bottles of 30 NDC 43598-745-30 Bottles of 90 NDC 43598-745-90 Bottles of 500 NDC 43598-745-05 Storage Store at 20 to 25°C (68 to 77°F) [See USP Controlled Room Temperature]. Keep container tightly closed. Dispense in a tight, light-resistant container as defined in the USP, with a child-resistant closure (as required).


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