Drug Facts
Composition & Profile
Identifiers & Packaging
HOW SUPPLIED Isosorbide Dinitrate Tablets, USP are available as follows: 10 mg oral, white, round, bisected tablets, debossed with “PAR 021” on one side and plain on the other side. Boxes of 10x10 UD 100, NDC 63739-569-10 20 mg oral, green, round, bisected tablets, debossed with “PAR 022” on one side and plain on the other side. Boxes of 10x10 UD 100, NDC 63739-367-10 Store at room temperature, approximately 25°C (77°F). Protect from light. Manufactured by: Par Pharmaceutical Chestnut Ridge, NY 10977 Distributed by: McKesson Corporation dba SKY Packaging Memphis, TN 38141 21457-1 February 2024; PACKAGE LABEL PRINCIPAL DISPLAY PANEL Isosorbide 20mg PACKAGE LABEL PRINCIPAL DISPLAY PANEL; PACKAGE LABEL PRINCIPAL DISPLAY PANEL Isosorbide 10mg PACKAGE LABEL PRINCIPAL DISPLAY PANEL
- HOW SUPPLIED Isosorbide Dinitrate Tablets, USP are available as follows: 10 mg oral, white, round, bisected tablets, debossed with “PAR 021” on one side and plain on the other side. Boxes of 10x10 UD 100, NDC 63739-569-10 20 mg oral, green, round, bisected tablets, debossed with “PAR 022” on one side and plain on the other side. Boxes of 10x10 UD 100, NDC 63739-367-10 Store at room temperature, approximately 25°C (77°F). Protect from light. Manufactured by: Par Pharmaceutical Chestnut Ridge, NY 10977 Distributed by: McKesson Corporation dba SKY Packaging Memphis, TN 38141 21457-1 February 2024
- PACKAGE LABEL PRINCIPAL DISPLAY PANEL Isosorbide 20mg PACKAGE LABEL PRINCIPAL DISPLAY PANEL
- PACKAGE LABEL PRINCIPAL DISPLAY PANEL Isosorbide 10mg PACKAGE LABEL PRINCIPAL DISPLAY PANEL
Overview
Isosorbide dinitrate, an organic nitrate, is a vasodilator with effects on both arteries and veins. The chemical name for isosorbide dinitrate is 1,4:3,6-dianhydro-D-glucitol 2, 5-dinitrate. The compound has the following structural formula: C 6 H 8 N 2 0 8 MW 236.14 Isosorbide dinitrate is a white, crystalline, odorless compound which is stable in air and in solution, has a melting point of 70°C and has an optical rotation of +134° (c=1.0, alcohol, 20°C). Isosorbide dinitrate is freely soluble in organic solvents such as acetone, alcohol, and ether, but is only sparingly soluble in water. Isosorbide dinitrate tablets are available for oral administration as 5 mg, 10 mg, 20 mg, or 30 mg tablets. Each tablet contains the following inactive ingredients: lactose anhydrous, magnesium stearate, microcrystalline cellulose, sodium starch glycolate and stearic acid. In addition, the 20 mg tablet contains D&C Yellow #10, FD&C Blue #1, and FD&C Yellow #6; the 30 mg tablet contains FD&C Blue #1. This is the structural formula
Indications & Usage
Isosorbide dinitrate tablets are indicated for the prevention of angina pectoris due to coronary artery disease. The onset of action of immediate-release oral isosorbide dinitrate is not sufficiently rapid for this product to be useful in aborting an acute anginal episode.
Dosage & Administration
As noted under " CLINICAL PHARMACOLOGY ," multiple-dose studies with isosorbide dinitrate and other nitrates have shown that maintenance of continuous 24-hour plasma levels results in refractory tolerance. Every dosing regimen for isosorbide dinitrate tablets must provide a daily dose-free interval to minimize the development of this tolerance. With immediate-release isosorbide dinitrate, it appears that one daily dose-free interval must be at least 14 hours long. As also noted under " CLINICAL PHARMACOLOGY ," the effects of the second and later doses have been smaller and shorter-lasting than the effects of the first. Large controlled studies with other nitrates suggest that no dosing regimen with isosorbide dinitrate tablets should be expected to provide more than about 12 hours of continuous anti-anginal efficacy per day. As with all titratable drugs, it is important to administer the minimum dose which produces the desired clinical effect. The usual starting dose of isosorbide dinitrate is 5 mg to 20 mg, two or three times daily. For maintenance therapy, 10 mg to 40 mg, two or three times daily is recommended. Some patients may require higher doses. A daily dose-free interval of at least 14 hours is advisable to minimize tolerance. The optimal interval will vary with the individual patient, dose and regimen.
Warnings & Precautions
WARNINGS Amplification of the vasodilatory effects of isosorbide dinitrate by sildenafil can result in severe hypotension. The time course and dose dependence of this interaction have not been studied. Appropriate supportive care has not been studied, but it seems reasonable to treat this as a nitrate overdose, with elevation of the extremities and with central volume expansion. The benefits of immediate-release oral isosorbide dinitrate in patients with acute myocardial infarction or congestive heart failure have not been established. If one elects to use isosorbide dinitrate in these conditions, careful clinical or hemodynamic monitoring must be used to avoid the hazards of hypotension and tachycardia. Because the effects of oral isosorbide dinitrate are so difficult to terminate rapidly, this formulation is not recommended in these settings.
Contraindications
Isosorbide dinitrate is contraindicated in patients who are allergic to isosorbide dinitrate or any of its other ingredients. Do not use isosorbide dinitrate in patients who are taking certain drugs for erectile dysfunction (phosphodiesterase inhibitors), such as sildenafil, tadalafil, or vardenafil. Concomitant use can cause severe hypotension, syncope, or myocardial ischemia. Do not use isosorbide dinitrate in patients who are taking the soluble guanylate cyclase stimulator riociguat. Concomitant use can cause hypotension.
Adverse Reactions
Adverse reactions to isosorbide dinitrate are generally dose-related, and almost all of these reactions are the result of isosorbide dinitrate's activity as a vasodilator. Headache, which may be severe, is the most commonly reported side effect. Headache may be recurrent with each daily dose, especially at higher doses. Transient episodes of lightheadedness, occasionally related to blood pressure changes, may also occur. Hypotension occurs infrequently, but in some patients it may be severe enough to warrant discontinuation of therapy. Syncope, crescendo angina, and rebound hypertension have been reported but are uncommon. Extremely rarely, ordinary doses of organic nitrates have caused methemoglobinemia in normal-seeming patients. Methemoglobinemia is so infrequent at these doses that further discussion of its diagnosis and treatment is deferred (see OVERDOSAGE ). Data are not available to allow estimation of the frequency of adverse reactions during treatment with isosorbide dinitrate tablets.
Drug Interactions
The vasodilating effects of isosorbide dinitrate may be additive with those of other vasodilators. Alcohol, in particular, has been found to exhibit additive effects of this variety. Concomitant use of isosorbide dinitrate with phosphodiesterase inhibitors in any form is contraindicated (see CONTRAINDICATIONS ). Concomitant use of isosorbide dinitrate with riociguat, a soluble guanylate cyclase stimulator, is contraindicated (see CONTRAINDICATIONS ).
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