Nitrostat NITROGLYCERIN PROFICIENT RX LP FDA Approved NITROSTAT is a stabilized sublingual compressed nitroglycerin tablet that contains 0.3 mg, 0.4 mg , or 0.6 mg nitroglycerin; as well as lactose monohydrate, NF; glyceryl monostearate, NF; pregelatinized starch, NF; calcium stearate, NF powder; and silicon dioxide, colloidal, NF. Nitroglycerin, an organic nitrate, is a vasodilating agent. The chemical name for nitroglycerin is 1, 2, 3 propanetriol trinitrate and the chemical structure is: Molecular weight: 227.09 Chemical Structure
Generic: NITROGLYCERIN
Mfr: PROFICIENT RX LP FDA Rx Only
FunFoxMeds bottle
Substance Nitroglycerin
Route
SUBLINGUAL
Applications
NDA021134
Package NDC

Drug Facts

Composition & Profile

Strengths
0.3 mg 0.4 mg 0.6 mg
Quantities
100 tablets 4 bottles 25 tablets
Treats Conditions
Indications And Usage Nitroglycerin Is Indicated For The Acute Relief Of An Attack Or Acute Prophylaxis Of Angina Pectoris Due To Coronary Artery Disease
Pill Appearance
Shape: round Color: white Imprint: N;4

Identifiers & Packaging

Container Type BOTTLE
All Product Codes
UNII
G59M7S0WS3
Packaging

HOW SUPPLIED NITROSTAT is supplied as white, round, flat-faced tablets in 3 strengths (0.3 mg, 0.4 mg, and 0.6 mg) in bottles containing 100 tablets each, with color-coded labels, and in color-coded Patient Convenience Packages of 4 bottles of 25 tablets each. 0.4 mg: Coded "N" on one side and "4" on the other. NDC 63187-884-25—Bottle of 25 Store at Controlled Room Temperature 20°–25°C (68°–77°F) [see USP].; PRINCIPAL DISPLAY PANEL - 0.4 mg Tablet Bottle Label ALWAYS DISPENSE WITH PATIENT PACKAGE INSERT NDC 63187-884-25 Nitrostat ® (Nitroglycerin Sublingual Tablets, USP) 0.4 mg / tablet 25 Sublingual Tablets Rx only 63187-884-25

Package Descriptions
  • HOW SUPPLIED NITROSTAT is supplied as white, round, flat-faced tablets in 3 strengths (0.3 mg, 0.4 mg, and 0.6 mg) in bottles containing 100 tablets each, with color-coded labels, and in color-coded Patient Convenience Packages of 4 bottles of 25 tablets each. 0.4 mg: Coded "N" on one side and "4" on the other. NDC 63187-884-25—Bottle of 25 Store at Controlled Room Temperature 20°–25°C (68°–77°F) [see USP].
  • PRINCIPAL DISPLAY PANEL - 0.4 mg Tablet Bottle Label ALWAYS DISPENSE WITH PATIENT PACKAGE INSERT NDC 63187-884-25 Nitrostat ® (Nitroglycerin Sublingual Tablets, USP) 0.4 mg / tablet 25 Sublingual Tablets Rx only 63187-884-25

Overview

NITROSTAT is a stabilized sublingual compressed nitroglycerin tablet that contains 0.3 mg, 0.4 mg , or 0.6 mg nitroglycerin; as well as lactose monohydrate, NF; glyceryl monostearate, NF; pregelatinized starch, NF; calcium stearate, NF powder; and silicon dioxide, colloidal, NF. Nitroglycerin, an organic nitrate, is a vasodilating agent. The chemical name for nitroglycerin is 1, 2, 3 propanetriol trinitrate and the chemical structure is: Molecular weight: 227.09 Chemical Structure

Indications & Usage

Nitroglycerin is indicated for the acute relief of an attack or acute prophylaxis of angina pectoris due to coronary artery disease.

Dosage & Administration

One tablet should be dissolved under the tongue or in the buccal pouch at the first sign of an acute anginal attack. The dose may be repeated approximately every 5 minutes until relief is obtained. If the pain persists after a total of 3 tablets in a 15-minute period, or if the pain is different than is typically experienced, prompt medical attention is recommended. NITROSTAT may be used prophylactically 5 to 10 minutes prior to engaging in activities that might precipitate an acute attack. During administration the patient should rest, preferably in the sitting position. No dosage adjustment is required in patients with renal failure.

Warnings & Precautions
WARNINGS The benefits of sublingual nitroglycerin in patients with acute myocardial infarction or congestive heart failure have not been established. If one elects to use nitroglycerin in these conditions, careful clinical or hemodynamic monitoring must be used because of the possibility of hypotension and tachycardia.
Contraindications

Nitroglycerin is contraindicated in patients who are allergic to it. Sublingual nitroglycerin therapy is contraindicated in patients with early myocardial infarction, severe anemia, increased intracranial pressure, and those with a known hypersensitivity to nitroglycerin. Administration of NITROSTAT is contraindicated in patients who are using a phosphodiesterase-5 (PDE-5) inhibitor (e.g., sildenafil citrate, tadalafil, vardenafil hydrochloride) since these compounds have been shown to potentiate the hypotensive effects of organic nitrates. Do not use NITROSTAT in patients who are taking the soluble guanylate cyclase stimulator riociguat. Concomitant use can cause hypotension.

Adverse Reactions

Headache that may be severe and persistent may occur immediately after use. Vertigo, dizziness, weakness, palpitation, and other manifestations of postural hypotension may develop occasionally, particularly in erect, immobile patients. Marked sensitivity to the hypotensive effects of nitrates (manifested by nausea, vomiting, weakness, diaphoresis, pallor, and collapse) may occur at therapeutic doses. Syncope due to nitrate vasodilatation has been reported. Flushing, drug rash, and exfoliative dermatitis have been reported in patients receiving nitrate therapy.

Drug Interactions

Concomitant use of NITROSTAT with soluble guanylate cyclase stimulators is contraindicated (see CONTRAINDICATIONS ). Concomitant use of nitrates and alcohol may cause hypotension. The vasodilatory and hemodynamic effects of nitroglycerin may be enhanced by concomitant administration of aspirin. Intravenous administration of nitroglycerin decreases the thrombolytic effect of alteplase. Therefore, caution should be observed in patients receiving sublingual nitroglycerin during alteplase therapy. Intravenous nitroglycerin reduces the anticoagulant effect of heparin and activated partial thromboplastin times (APTT) should be monitored in patients receiving heparin and intravenous nitroglycerin. It is not known if this effect occurs following single sublingual nitroglycerin doses. Tricyclic antidepressants (amitriptyline, desipramine, doxepin, others) and anticholinergic drugs may cause dry mouth and diminished salivary secretions. This may make dissolution of sublingual nitroglycerin difficult. Increasing salivation with chewing gum or artificial saliva products may prove useful in aiding dissolution of sublingual nitroglycerin. Oral administration of nitroglycerin markedly decreases the first-pass metabolism of dihydroergotamine and subsequently increases its oral bioavailability. Ergotamine is known to precipitate angina pectoris. Therefore, patients receiving sublingual nitroglycerin should avoid ergotamine and related drugs or be monitored for symptoms of ergotism if this is not possible. Administration of nitroglycerin is contraindicated in patients who are using PDE-5 inhibitors (e.g., sildenafil citrate, tadalafil, vardenafil hydrochloride). These compounds have been shown to potentiate the hypotensive effects of organic nitrates. A decrease in therapeutic effect of sublingual nitroglycerin may result from use of long-acting nitrates.

Storage & Handling

Store at Controlled Room Temperature 20°–25°C (68°–77°F) [see USP].


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