Benzonatate BENZONATATE BRYANT RANCH PREPACK 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 contains: Benzonatate, USP 100 mg Each benzonatate capsule USP contains: Benzonatate, USP 150 mg Each benzonatate capsule USP contains: Benzonatate, USP 200 mg Benzonatate capsules USP also contain: bloom gelatin, glycerin, purified water, medium chain triglycerides, lecithin, isopropyl alcohol, nitrogen. 100 mg and 200 mg capsules also contain D&C Yellow No. 10. 150 mg capsules also contain FD&C Yellow No. 6 powder. Each capsule also contains black iron oxide, propylene glycol, hypromellose as imprinting ink.

Drug Facts

Composition & Profile

Quantities
30 capsules 100 capsules 45 capsules 20 capsules 15 capsules 21 capsules 60 capsules 50 capsules 90 capsules 6 capsules
Treats Conditions
Indications And Usage Benzonatate Capsules Is Indicated For The Symptomatic Relief Of Cough

Identifiers & Packaging

Container Type BOTTLE
UNII
5P4DHS6ENR
Packaging

HOW SUPPLIED NDC: 71335-2486-1: 30 Capsules in a BOTTLE NDC: 71335-2486-2: 100 Capsules in a BOTTLE NDC: 71335-2486-3: 45 Capsules in a BOTTLE NDC: 71335-2486-4: 20 Capsules in a BOTTLE NDC: 71335-2486-5: 15 Capsules in a BOTTLE NDC: 71335-2486-6: 21 Capsules in a BOTTLE NDC: 71335-2486-7: 60 Capsules in a BOTTLE NDC: 71335-2486-8: 50 Capsules in a BOTTLE NDC: 71335-2486-9: 90 Capsules in a BOTTLE NDC: 71335-2486-0: 6 Capsules in a BOTTLE; Benzonatate 200mg Capsule Label

Package Descriptions
  • HOW SUPPLIED NDC: 71335-2486-1: 30 Capsules in a BOTTLE NDC: 71335-2486-2: 100 Capsules in a BOTTLE NDC: 71335-2486-3: 45 Capsules in a BOTTLE NDC: 71335-2486-4: 20 Capsules in a BOTTLE NDC: 71335-2486-5: 15 Capsules in a BOTTLE NDC: 71335-2486-6: 21 Capsules in a BOTTLE NDC: 71335-2486-7: 60 Capsules in a BOTTLE NDC: 71335-2486-8: 50 Capsules in a BOTTLE NDC: 71335-2486-9: 90 Capsules in a BOTTLE NDC: 71335-2486-0: 6 Capsules in a BOTTLE
  • Benzonatate 200mg Capsule Label

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 contains: Benzonatate, USP 100 mg Each benzonatate capsule USP contains: Benzonatate, USP 150 mg Each benzonatate capsule USP contains: Benzonatate, USP 200 mg Benzonatate capsules USP also contain: bloom gelatin, glycerin, purified water, medium chain triglycerides, lecithin, isopropyl alcohol, nitrogen. 100 mg and 200 mg capsules also contain D&C Yellow No. 10. 150 mg capsules also contain FD&C Yellow No. 6 powder. Each capsule also contains black iron oxide, propylene glycol, hypromellose as imprinting ink.

Indications & Usage

Benzonatate capsules is indicated for the symptomatic relief of cough.

Dosage & Administration

Adults and Children over 10 years of age: Usual dose is one 100 mg, 150 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. B enzonatate 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 capsules 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. Der m atologic: 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.


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