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Ramipril 2.5 MG Oral Capsule

1 INDICATIONS AND USAGE Ramipril capsules are an angiotensin converting enzyme (ACE) inhibitor indicated for the treatment of hypertension, to lower blood pressure. Lowering blood pressure reduces the risk of fatal and nonfatal cardiovascular events, primarily strokes and myocardial infarctions. It may be used alone or in combination with thiazide diuretics ( 1.1 ). In patients 55 years or older at high risk of developing a major cardiovascular event, ramipril capsules are indicated to reduce the risk of myocardial infarction, stroke, or death from cardiovascular causes ( 1.2 ). Ramipril capsules are indicated in stable patients who have demonstrated clinical signs of congestive heart failure post-myocardial infarction ( 1.3 ). 1.1 hypertension Ramipril capsules are indicated for the treatment of hypertension, to lower blood pressure. Lowering blood pressure reduces the risk of fatal and nonfatal cardiovascular events, primarily strokes and myocardial infarctions. These benefits have been seen in controlled trials of antihypertensive drugs from a wide variety of pharmacologic classes including this drug. Control of high blood pressure should be part of comprehensive cardiovascular risk management, including, as appropriate, lipid control, diabetes management, antithrombotic therapy, smoking cessation, exercise, and limited sodium intake. Many patients will require more than one drug to achieve blood pressure goals. For specific advice on goals and management, see published guidelines, such as those of the National High Blood Pressure Education Program’s Joint National Committee on Prevention, Detection, Evaluation, and Treatment of High Blood Pressure (JNC). Numerous antihypertensive drugs, from a variety of pharmacologic classes and with different mechanisms of action, have been shown in randomized controlled trials to reduce cardiovascular morbidity and mortality, and it can be concluded that it is blood pressure reduction, and not some other pharmacologic property of the drugs, that is largely responsible for those benefits. The largest and most consistent cardiovascular outcome benefit has been a reduction in the risk of stroke, but reductions in myocardial infarction and cardiovascular mortality also have been seen regularly. Elevated systolic or diastolic pressure causes increased cardiovascular risk, and the absolute risk increase per mmHg is greater at higher blood pressures, so that even modest reductions of severe hypertension can provide substantial benefit. Relative risk reduction from blood pressure reduction is similar across populations with varying absolute risk, so the absolute benefit is greater in patients who are at higher risk independent of their hypertension (for example, patients with diabetes or hyperlipidemia), and such patients would be expected to benefit from more aggressive treatment to a lower blood pressure goal. Some antihypertensive drugs have smaller blood pressure effects (as monotherapy) in black patients, and many antihypertensive drugs have additional approved indications and effects (e.g., on angina, heart failure, or diabetic kidney disease). These considerations may guide selection of therapy. Ramipril capsules may be used alone or in combination with thiazide diuretics. 1.2 Reduction in the Risk of Myocardial Infarction, Stroke, and Death from Cardiovascular Causes Ramipril capsules are indicated in patients 55 years or older at high risk of developing a major cardiovascular event because of a history of coronary artery disease, stroke, peripheral vascular disease, or diabetes that is accompanied by at least one other cardiovascular risk factor (hypertension, elevated total cholesterol levels, low HDL levels, cigarette smoking, or documented microalbuminuria), to reduce the risk of myocardial infarction, stroke, or death from cardiovascular causes. Ramipril capsules can be used in addition to other needed treatment (such as antihypertensive, antiplatelet, or lipid-lowering therapy) [see Clinical Studies (14.2) ]. 1.3 Heart Failure Post-Myocardial Infarction Ramipril capsules are indicated in stable patients who have demonstrated clinical signs of congestive heart failure within the first few days after sustaining acute myocardial infarction. Administration of ramipril capsules to such patients have been shown to decrease the risk of death (principally cardiovascular death) and to decrease the risks of failure-related hospitalization and progression to severe/resistant heart failure [see Clinical Studies (14.3) ] .

Aurobindo Pharma Limited


8 months ago CAPSULE ORANGE D 06 Ramipril 2.5 MG Oral Capsule

CAPSULE ORANGE D 06

8 months ago CAPSULE ORANGE D 06 Ramipril 2.5 MG Oral Capsule

D 06 CAPSULE ORANGE

16 HOW SUPPLIED/STORAGE AND HANDLING

RAMIPRIL capsules USP , 1.25 mg are yellow/yellow size β€˜4’ hard gelatin capsules imprinted with β€˜D’ on yellow cap and β€˜05’ on yellow body with black edible ink filled with white to almost white powder. Bottles of 30 NDC 65862-474-30 Bottles of 100 NDC 65862-474-01 Bottles of 1,000 NDC 65862-474-99 10 x 10 Unit-dose capsules NDC 65862-474-10

RAMIPRIL capsules USP , 2.5 mg are orange/orange size β€˜4’ hard gelatin capsules imprinted with β€˜D’ on orange cap and β€˜06’ on orange body with black edible ink filled with white to almost white powder. Bottles of 30 NDC 65862-475-30 Bottles of 100 NDC 65862-475-01 Bottles of 500 NDC 65862-475-05 Bottles of 1,000 NDC 65862-475-99 10 x 10 Unit-dose capsules NDC 65862-475-10

RAMIPRIL capsules USP , 5 mg are red/red size β€˜4’ hard gelatin capsules imprinted with β€˜D’ on red cap and β€˜07’ on red body with black edible ink filled with white to almost white powder. Bottles of 30 NDC 65862-476-30 Bottles of 100 NDC 65862-476-01 Bottles of 500 NDC 65862-476-05 Bottles of 1,000 NDC 65862-476-99 10 x 10 Unit-dose capsules NDC 65862-476-10

RAMIPRIL capsules USP , 10 mg are blue/blue size β€˜4’ hard gelatin capsules imprinted with β€˜D’ on blue cap and β€˜08’ on blue body with black edible ink filled with white to almost white powder. Bottles of 30 NDC 65862-477-30 Bottles of 100 NDC 65862-477-01 Bottles of 500 NDC 65862-477-05 Bottles of 1,000 NDC 65862-477-99 10 x 10 Unit-dose capsules NDC 65862-477-10 Store at 20Β° to 25Β°C (68Β° to 77Β°F). [See USP Controlled Room Temperature.] Dispense in well-closed container with safety closure.


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