Benzonatate BENZONATATE ST. MARY'S MEDICAL PARK PHARMACY FDA Approved Benzonatate, a non-narcotic oral antitussive agent, is 2, 5, 8, 11, 14, 17, 20, 23, 26-nonaoxaoctacosan-28-yl p-(butylamino) benzoate; with a molecular weight of 603.7. Each benzonatate capsule USP,100 mg contains: Benzonatate, USP 100 mg. Each benzonatate capsule USP,200 mg contains: Benzonatate, USP 200 mg. Benzonatate Capsules USP also contain: D&C Yellow 10, gelatin, glycerin, methylparaben, propylparaben, shellac and titanium dioxide. Chemical Structure
FunFoxMeds bottle
Substance Benzonatate
Route
ORAL
Applications
ANDA202765

Drug Facts

Composition & Profile

Strengths
100 mg
Quantities
15 bottles 30 bottles
Treats Conditions
Indications And Usage Benzonatate Capsule Is Indicated For The Symptomatic Relief Of Cough
Pill Appearance
Shape: oval Color: yellow Imprint: 1

Identifiers & Packaging

Container Type BOTTLE
UNII
5P4DHS6ENR
Packaging

HOW SUPPLIED Benzonatate Capsules USP, 100 mg are available as yellow, oval soft gelatin capsules with‘1’imprinted in white ink. NDC 60760-869-15 BOTTLES OF 15 NDC 60760-869-30 BOTTLES OF 30 Store at 20° to 25°C (68° to 77°F) excursions permitted between 15° to 30°C (59° to 86°F) [see USP Controlled Room Temperature]. PROTECT FROM LIGHT; 869-30

Package Descriptions
  • HOW SUPPLIED Benzonatate Capsules USP, 100 mg are available as yellow, oval soft gelatin capsules with‘1’imprinted in white ink. NDC 60760-869-15 BOTTLES OF 15 NDC 60760-869-30 BOTTLES OF 30 Store at 20° to 25°C (68° to 77°F) excursions permitted between 15° to 30°C (59° to 86°F) [see USP Controlled Room Temperature]. PROTECT FROM LIGHT
  • 869-30

Overview

Benzonatate, a non-narcotic oral antitussive agent, is 2, 5, 8, 11, 14, 17, 20, 23, 26-nonaoxaoctacosan-28-yl p-(butylamino) benzoate; with a molecular weight of 603.7. Each benzonatate capsule USP,100 mg contains: Benzonatate, USP 100 mg. Each benzonatate capsule USP,200 mg contains: Benzonatate, USP 200 mg. Benzonatate Capsules USP also contain: D&C Yellow 10, gelatin, glycerin, methylparaben, propylparaben, shellac and titanium dioxide. Chemical Structure

Indications & Usage

Benzonatate Capsule is indicated for the symptomatic relief of cough.

Dosage & Administration

Adults and Children over 10 years of age Usual dose is one 100 mg or 200 mg capsule three times a day as needed for cough. If necessary to control cough, up to 600 mg daily in three divided doses may be given. Benzonatate Capsules should be swallowed whole. Benzonatate Capsules are not to be broken, chewed, dissolved, cut or crushed.

Warnings & Precautions
WARNINGS Hypersensitivity Severe hypersensitivity reactions (including bronchospasm, laryngospasm and cardiovascular collapse) have been reported which are possibly related to local anesthesia from sucking or chewing the capsule instead of swallowing it. Severe reactions have required intervention with vasopressor agents and supportive measures. Psychiatric Effects Isolated instances of bizarre behavior, including mental confusion and visual hallucinations, have also been reported in patients taking Benzonatate Capsule in combination with other prescribed drugs. Accidental Ingestion and Death in Children Keep Benzonatate Capsules out of reach of children. Accidental ingestion of Benzonatate Capsules resulting in death has been reported in children below age 10. Signs and symptoms of overdose have been reported within 15-20 minutes and death has been reported within one hour of ingestion. If accidental ingestion occurs, seek medical attention immediately (see OVERDOSAGE ).
Contraindications

Hypersensitivity to benzonatate or related compounds.

Adverse Reactions

Potential Adverse Reactions to Benzonatate Capsules may include: Hypersensitivity reactions including bronchospasm, laryngospasm,cardiovascular collapse possibly related to local anesthesia from chewing or sucking the capsule. CNS: sedation; headache; dizziness; mental confusion; visual hallucinations. GI: constipation; nausea; GI upset. Dermatologic: pruritus; skin eruptions. Other: nasal congestion; sensation of burning in the eyes; vague "chilly" sensation; numbness of the chest; hypersensitivity. Deliberate or accidental overdose has resulted in death, particularly in children.

Storage & Handling

Store at 20° to 25°C (68° to 77°F) excursions permitted between 15° to 30°C (59° to 86°F) [see USP Controlled Room Temperature]. PROTECT FROM LIGHT


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