ISOSORBIDE DINITRATE ISOSORBIDE DINITRATE REMEDYREPACK INC. FDA Approved Isosorbide dinitrate (ISDN) is 1,4:3,6-dianhydro-D-glucitol 2,5-dinitrate, an organic nitrate whose structural formula is and whose molecular weight is 236.14. The organic nitrates are vasodilators, active on both arteries and veins. Isosorbide dinitrate is a white, crystalline powder compound which is stable in air and in solution, has a melting point of 69°C to 72°C and optically active. Isosorbide dinitrate is very soluble in acetone, sparingy soluble in alcohol and very slightly soluble in water. Each Isosorbide dinitrate tablet contains 5 mg, 10 mg, 20 mg, 30 mg or 40 mg of isosorbide dinitrate. The inactive ingredients in each tablet are microcrystalline cellulose, colloidal silicon dioxide, and magnesium stearate. The 5mg, 10 mg, 20 mg and 30 mg dosage strengths also contain anhydrous lactose and sodium starch glycolate Type A. Additionally 5 mg contains FD & C red 40 Al lake. 10 mg, 20mg, 30 mg and 40 mg contains FD & C Blue 1 Al lake and D & C Yellow 10 Al lake. FDA approved dissolution test specifications differ from USP. Isosorbide Dinitrate Chemical Structure
FunFoxMeds bottle
Route
ORAL
Applications
ANDA215723
Product NDC
Package NDC

Drug Facts

Composition & Profile

Strengths
10 mg
Quantities
00 pack 22 pack
Treats Conditions
Indications And 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
Pill Appearance
Shape: round Color: green Imprint: UpArrowhead22

Identifiers & Packaging

Container Type BOTTLE
All Product Codes
UNII
IA7306519N
Packaging

HOW SUPPLIED Isosorbide dinitrate Tablets are available as follows: 10 mg, Light green to green mottled round tablets, debossed with, "Λ" on one side and score line on the other side. NDC: 70518-4405-00 PACKAGING: 30 in 1 BLISTER PACK Store at 20° to 25°C (68° to 77°F); excursions permitted to 15° to 30°C (59° to 86°F) [see USP Controlled Room Temperature]. Protect from light. Keep bottles tightly closed. Dispense in a light-resistant, tight container. All trademarks are the property of their respective owners. Repackaged and Distributed By: Remedy Repack, Inc. 625 Kolter Dr. Suite #4 Indiana, PA 1-724-465-8762; DRUG: ISOSORBIDE DINITRATE GENERIC: isosorbide dinitrate DOSAGE: TABLET ADMINSTRATION: ORAL NDC: 70518-4405-0 COLOR: green SHAPE: ROUND SCORE: Two even pieces SIZE: 6 mm IMPRINT: UpArrowhead22 PACKAGING: 30 in 1 BLISTER PACK ACTIVE INGREDIENT(S): ISOSORBIDE DINITRATE 10mg in 1 INACTIVE INGREDIENT(S): MICROCRYSTALLINE CELLULOSE SILICON DIOXIDE MAGNESIUM STEARATE ANHYDROUS LACTOSE SODIUM STARCH GLYCOLATE TYPE A FD&C BLUE NO. 1 ALUMINUM LAKE D&C YELLOW NO. 10 ALUMINUM LAKE Remedy_Label

Package Descriptions
  • HOW SUPPLIED Isosorbide dinitrate Tablets are available as follows: 10 mg, Light green to green mottled round tablets, debossed with, "Λ" on one side and score line on the other side. NDC: 70518-4405-00 PACKAGING: 30 in 1 BLISTER PACK Store at 20° to 25°C (68° to 77°F); excursions permitted to 15° to 30°C (59° to 86°F) [see USP Controlled Room Temperature]. Protect from light. Keep bottles tightly closed. Dispense in a light-resistant, tight container. All trademarks are the property of their respective owners. Repackaged and Distributed By: Remedy Repack, Inc. 625 Kolter Dr. Suite #4 Indiana, PA 1-724-465-8762
  • DRUG: ISOSORBIDE DINITRATE GENERIC: isosorbide dinitrate DOSAGE: TABLET ADMINSTRATION: ORAL NDC: 70518-4405-0 COLOR: green SHAPE: ROUND SCORE: Two even pieces SIZE: 6 mm IMPRINT: UpArrowhead22 PACKAGING: 30 in 1 BLISTER PACK ACTIVE INGREDIENT(S): ISOSORBIDE DINITRATE 10mg in 1 INACTIVE INGREDIENT(S): MICROCRYSTALLINE CELLULOSE SILICON DIOXIDE MAGNESIUM STEARATE ANHYDROUS LACTOSE SODIUM STARCH GLYCOLATE TYPE A FD&C BLUE NO. 1 ALUMINUM LAKE D&C YELLOW NO. 10 ALUMINUM LAKE Remedy_Label

Overview

Isosorbide dinitrate (ISDN) is 1,4:3,6-dianhydro-D-glucitol 2,5-dinitrate, an organic nitrate whose structural formula is and whose molecular weight is 236.14. The organic nitrates are vasodilators, active on both arteries and veins. Isosorbide dinitrate is a white, crystalline powder compound which is stable in air and in solution, has a melting point of 69°C to 72°C and optically active. Isosorbide dinitrate is very soluble in acetone, sparingy soluble in alcohol and very slightly soluble in water. Each Isosorbide dinitrate tablet contains 5 mg, 10 mg, 20 mg, 30 mg or 40 mg of isosorbide dinitrate. The inactive ingredients in each tablet are microcrystalline cellulose, colloidal silicon dioxide, and magnesium stearate. The 5mg, 10 mg, 20 mg and 30 mg dosage strengths also contain anhydrous lactose and sodium starch glycolate Type A. Additionally 5 mg contains FD & C red 40 Al lake. 10 mg, 20mg, 30 mg and 40 mg contains FD & C Blue 1 Al lake and D & C Yellow 10 Al lake. FDA approved dissolution test specifications differ from USP. Isosorbide Dinitrate Chemical Structure

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 ISDN 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 ISDN, 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 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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