Simvastatin 10 mg
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. In patients with coronary heart disease (CHD) or at high risk of CHD, simvastatin can be started simultaneously with diet. Simvastatin is an HMG-CoA reductase inhibitor (statin) indicated as an adjunctive therapy to diet to: β’ Reduce the risk of total mortality by reducing CHD deaths and reduce the risk of non-fatal myocardial infarction, stroke, and the need for revascularization procedures in patients at high risk of coronary events. (1.1) β’ Reduce elevated total-C, LDL-C, Apo B, TG and increase HDL-C in patients with primary hyperlipidemia (heterozygous familial and nonfamilial) and mixed dyslipidemia. (1.2) β’ Reduce elevated TG in patients with hypertriglyceridemia and reduce TG and VLDL-C in patients with primary dysbetaβ lipoproteinemia. (1.2) β’ Reduce total-C and LDL-C in adult patients with homozygous familial hypercholesterolemia. (1.2) β’ Reduce elevated total-C, LDL-C, and Apo B in boys and postmenarchal girls, 10 to 17 years of age with heterozygous familial hypercholesterolemia after failing an adequate trial of diet therapy. (1.2, 1.3) Limitations of Use Simvastatin has not been studied in Fredrickson Types I and V dyslipidemias. (1.4) 1.1 Reductions in Risk of CHD Mortality and Cardiovascular Events In patients at high risk of coronary events because of existing coronary heart disease, diabetes, peripheral vessel disease, history of stroke or other cerebrovascular disease, simvastatin is indicated to: β’ Reduce the risk of total mortality by reducing CHD deaths. β’ Reduce the risk of non-fatal myocardial infarction and stroke. β’ Reduce the need for coronary and non-coronary revascularization procedures. 1.2 hyperlipidemia Simvastatin is indicated to: β’ Reduce elevated total cholesterol (total-C), low-density lipoprotein cholesterol (LDL-C), apolipoprotein B (Apo B), and triglycerides (TG), and to increase high-density lipoprotein cholesterol (HDL-C) in patients with primary hyperlipidemia (Fredrickson type IIa, heterozygous familial and nonfamilial) or mixed dyslipidemia (Fredrickson type IIb). β’ Reduce elevated TG in patients with hypertriglyceridemia (Fredrickson type lV hyperlipidemia). β’ Reduce elevated TG and VLDL-C in patients with primary dysbetalipoproteinemia (Fredrickson type lll hyperlipidemia). β’ Reduce total-C and LDL-C in patients with homozygous familial hypercholesterolemia (HoFH) as an adjunct to other lipid-lowering treatments (e.g., LDL apheresis) or if such treatments are unavailable. 1.3 Adolescent Patients with Heterozygous Familial hypercholesterolemia (HeFH) Simvastatin is indicated as an adjunct to diet to reduce total-C, LDL-C, and Apo B levels in adolescent boys and girls who are at least one year post-menarche, 10 to 17 years of age, with HeFH, if after an adequate trial of diet therapy the following findings are present: 1. LDL cholesterol remains β₯190 mg/dL; or 2. LDL cholesterol remains β₯160 mg/dL and β’ There is a positive family history of premature cardiovascular disease (CVD) or β’ Two or more other CVD risk factors are present in the adolescent patient. The minimum goal of treatment in pediatric and adolescent patients is to achieve a mean LDL-C <130 mg/dL. The optimal age at which to initiate lipid-lowering therapy to decrease the risk of symptomatic adulthood CAD has not been determined. 1.4 Limitations of Use Simvastatin has not been studied in conditions where the major abnormality is elevation of chylomicrons (i.e., hyperlipidemia Fredrickson types I and V).
Blu Pharmaceuticals, LLC
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Blu Pharmaceuticals, LLC
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16 HOW SUPPLIED Simvastatin Tablets USP 5 mg are white to off white, oval, biconvex, film-coated tablets with βB300β debossed on one side and β5β on the other side. They are supplied as follows: NDC 24658-300-30 bottles of 30 NDC 24658-300-45 bottles of 45. NDC 24658-300-90 bottles of 90 NDC 24658-300-10 bottles of 1000 Simvastatin Tablets USP 10 mg are peach to dark peach, oval, biconvex, film-coated tablets with βB301βdebossed on one side and β10β on the other side. They are supplied as follows: NDC 24658-301-15 bottles of 15 NDC 24658-301-30 bottles of 30 NDC 24658-301-45 bottles of 45 NDC 24658-301-90 bottles of 90 NDC 24658-301-10 bottles of 1000. Simvastatin Tablets USP 20 mg are orange to dark orange, oval, biconvex, film-coated tablets with βB302β debossed on one side and β20β on the other side. They are supplied as follows: NDC 24658-302-15 bottles of 15 NDC 24658-302-30 bottles of 30 NDC 24658-302-45 bottles of 45 NDC 24658-302-90 bottles of 90. NDC 24658-302-10 bottles of 1000 Simvastatin Tablets USP 40 mg are light pink to pink, oval, biconvex, film-coated tablets with βB303β debossed on one side and β40β on the other side. They are supplied as follows: NDC 24658-303-15 bottles of 15 NDC 24658-303-30 bottles of 30 NDC 24658-303-45 bottles of 45 NDC 24658-303-90 bottles of 90. NDC 24658-303-10 bottles of 1000 Simvastatin Tablets USP 80 mg are dark pink to pink, capsule-shaped, film-coated tablets with βB304β debossed on one side and β80β on the other side. They are supplied as follows: NDC 24658-304-15 bottles of 15 NDC 24658-304-30 bottles of 30 NDC 24658-304-45 bottles of 45 NDC 24658-304-90 bottles of 90 NDC 24658-304-10 bottles of 1000. Storage Store between 20 to 25Β°C (68 to 77Β°F). Dispense in a tightly-closed container
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