NITROGLYCERIN tablet

Country: United States

Language: English

Source: NLM (National Library of Medicine)

Active ingredient:

NITROGLYCERIN (UNII: G59M7S0WS3) (NITROGLYCERIN - UNII:G59M7S0WS3)

Available from:

Bryant Ranch Prepack

Administration route:

SUBLINGUAL

Prescription type:

PRESCRIPTION DRUG

Therapeutic indications:

Nitroglycerin sublingual tablets are indicated for the acute relief of an attack or acute prophylaxis of angina pectoris due to coronary artery disease. Do not use nitroglycerin sublingual tablets in patients who are taking PDE-5 Inhibitors, such as avanafil, sildenafil, tadalafil, vardenafil hydrochloride. Concomitant use can cause severe hypotension, syncope, or myocardial ischemia [see Drug Interactions (7.1)]. Do not use nitroglycerin sublingual tablets in patients who are taking the soluble guanylate cyclase stimulators, such as riociguat. Concomitant use can cause hypotension. Nitroglycerin sublingual tablets are contraindicated in patients with severe anemia (large doses of nitroglycerin may cause oxidation of hemoglobin to methemoglobin and could exacerbate anemia). Nitroglycerin sublingual tablets may precipitate or aggravate increased intracranial pressure and thus should not be used in patients with possible increased intracranial pressure (e.g., cerebral hemorrhage or traumatic brain injury). Nitr

Product summary:

Nitroglycerin sublingual tablets, USP are supplied in strengths in color-coded labeled bottles containing 100 tablets each (0.3 mg). The 0.3 mg sublingual tablets are a white, round, flat faced tablet debossed with “3” on one side and “V” on other side. They are supplied as: NDC: 63629-8828-1 Bottle of 100 tablets Store at 20° to 25°C (68° to 77°F) [see USP Controlled Room Temperature]. Nitroglycerin should be kept in the original glass container and must be tightly capped after each use to prevent loss of tablet potency.

Authorization status:

Abbreviated New Drug Application

Summary of Product characteristics

NITROGLYCERIN- NITROGLYCERIN TABLET
BRYANT RANCH PREPACK
----------
HIGHLIGHTS OF PRESCRIBING INFORMATION
THESE HIGHLIGHTS DO NOT INCLUDE ALL THE INFORMATION NEEDED TO USE
NITROGLYCERIN
SUBLINGUAL TABLETS SAFELY AND EFFECTIVELY. SEE FULL PRESCRIBING
INFORMATION FOR
NITROGLYCERIN SUBLINGUAL TABLETS.
NITROGLYCERIN SUBLINGUAL TABLETS, FOR ORAL USE
INITIAL U.S. APPROVAL: 1981
INDICATIONS AND USAGE
Nitroglycerin sublingual tablets are a nitrate vasodilator indicated
for relief of an attack or prophylaxis of
angina pectoris due to coronary artery disease. (1)
DOSAGE AND ADMINISTRATION
• At the onset of an attack, administer one tablet under the tongue
or buccal pouch. One additional tablet
may be administered every 5 minutes as needed. No more than 3 total
tablets are recommended within a
15 minute period. (2)
• If chest pain persists after three tablets, seek prompt medical
attention. (2)
• May be used prophylactically 5 to 10 minutes prior to engaging in
activities that might precipitate an
acute attack. (2)
DOSAGE FORMS AND STRENGTHS
Sublingual tablets, 0.3 mg; 0.4 mg; 0.6 mg (3)
CONTRAINDICATIONS
• Use of phosphodiesterase type 5 (PDE-5) inhibitors, such as
avanafil, sildenafil, tadalafil, or vardenafil, or
soluble guanylate cyclase (sGC) stimulators. (4.1, 7.1)
• Severe anemia (4.2)
• Increased intracranial pressure (4.3)
• Hypersensitivity to nitroglycerin sublingual tablets or to other
nitrates or nitrites or any excipient (4.4)
• Circulatory failure and shock (4.5)
WARNINGS AND PRECAUTIONS
• Tolerance: Excessive use may lead to tolerance. (5.1)
• Hypotension: Severe hypotension may occur. (5.2)
ADVERSE REACTIONS
Most common adverse reactions occurring at a frequency greater than 2%
are headache, dizziness and
paresthesia. (6)
TO REPORT SUSPECTED ADVERSE REACTIONS, CONTACT ALVOGEN, INC. AT
1-866-770-3024 OR FDA
AT 1-800-FDA-1088 OR WWW.FDA.GOV/MEDWATCH.
DRUG INTERACTIONS
Ergotamine: increased bioavailability of ergotamine. Avoid concomitant
use. (7.2)
SEE 17 FOR PATIENT COUNSELING INFORMATION