Product image of Montelukast Teva (Montelukast Sodium) supplied by GNH India

Montelukast Teva

Active Ingredient:
Montelukast Sodium
Origin:
EU

Montelukast Teva (Montelukast Sodium)

Montelukast Sodium, the active ingredient in Montelukast Teva, is a leukotriene receptor antagonist presented as an oral tablet for oral use. It treats asthma, allergic rhinitis and exercise‑induced bronchoconstriction in adults and children.

GNH India supplies Montelukast Teva as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Teva Pharmaceuticals Slovakia S.R.O

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Indications & Clinical Uses

Montelukast Teva is a leukotriene receptor antagonist used in the management of several respiratory allergic conditions.

  • Asthma: improves control of chronic airway inflammation and reduces frequency of exacerbations.
  • Allergic rhinitis: relieves nasal congestion, sneezing and itching caused by seasonal or perennial allergens.
  • Exercise‑induced bronchoconstriction: prevents airway narrowing that occurs during or after physical activity.

How It Works

  • Montelukast selectively blocks the cysteinyl leukotriene receptor CysLT1, preventing leukotriene D4 from binding. This inhibition reduces leukotriene‑mediated bronchoconstriction, mucus secretion, vascular permeability, and inflammatory cell recruitment in the airways, thereby improving respiratory function and symptom control.

Side Effects

Montelukast is generally well tolerated, but adverse reactions can occur.

Common Side Effects

  • Headache: mild to moderate pain often transient.
  • Abdominal pain: discomfort or cramps in the stomach region.
  • Nausea: feeling of queasiness without vomiting.
  • Dizziness: light‑headed sensation, especially on standing.
  • Fatigue: unusual tiredness or lack of energy.
  • Cough: mild irritation of the throat.

Serious or Rare Side Effects

  • Allergic reactions: rash, angioedema, or hives requiring medical attention.
  • Neuropsychiatric events: mood changes, agitation, or suicidal thoughts.
  • Hepatic enzyme elevation: abnormal liver function tests observed in laboratory monitoring.

Precautions & Warnings

When prescribing Montelukast, clinicians should consider several safety aspects.

  • Monitor liver function: periodic testing is advised for patients with hepatic disease.
  • Caution in psychiatric history: observe for mood alterations or suicidal ideation.
  • Avoid in known hypersensitivity: discontinue if allergic reaction occurs.
  • Adjust in renal impairment: dose may need modification in severe kidney disease.
  • Pregnancy and lactation: use only if potential benefit outweighs risk.
  • Store at room temperature: keep in the original pack, protect from moisture and direct sunlight.

Avoid Interactions

Montelukast may interact with other medicines, affecting efficacy or safety.

Major Interactions (Avoid)

  • Strong CYP3A4 inhibitors (e.g., ketoconazole): may increase systemic exposure.
  • Rifampin or other enzyme inducers: can markedly reduce therapeutic effect.

Moderate Interactions (Monitor Closely)

  • Antidepressants (SSRIs, SNRIs): may heighten risk of neuropsychiatric side effects.
  • NSAIDs: combined use may increase gastrointestinal discomfort.
  • Theophylline: additive bronchodilator effect may require dose adjustment.

Frequently Asked Questions

Montelukast Teva is prescribed to manage asthma, allergic rhinitis and exercise‑induced bronchoconstriction. By blocking leukotriene receptors, it helps control airway inflammation, reduces nasal allergy symptoms, and prevents bronchospasm triggered by physical activity.

The drug selectively antagonizes the cysteinyl leukotriene receptor CysLT1. This blocks leukotriene D4 from causing bronchoconstriction, mucus production, and inflammatory cell recruitment, leading to improved airway patency and reduced allergic inflammation.

The appropriate dose is determined by the prescribing healthcare professional based on the patient’s age, weight, indication and clinical response. Patients should follow the exact regimen provided on the prescription label.

Safety data are limited; Montelukast should only be used during pregnancy or lactation if the potential benefit justifies any possible risk to the fetus or infant. The prescriber will evaluate individual circumstances before recommending therapy.

Submit an enquiry on the product page at gnhindia.com, specifying the required quantity. GNH India works with hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details and any necessary import documentation.

Montelukast belongs to the leukotriene receptor antagonist class, offering an oral alternative to inhaled corticosteroids or long‑acting beta‑agonists. It is particularly useful for patients with allergic components or those who experience exercise‑induced bronchoconstriction, though it may be used as add‑on therapy rather than a sole controller in severe asthma.

Store the tablets at room temperature, below 25 °C, in the original packaging. Keep them away from moisture, direct sunlight and excessive heat to maintain product stability.

Montelukast Teva is taken orally, usually once daily, with or without food. The tablet should be swallowed whole with water and not chewed or crushed unless otherwise instructed by a healthcare professional.

Serious concerns include rare allergic reactions such as rash or angioedema, and neuropsychiatric events like mood changes, agitation or suicidal thoughts. Patients should seek immediate medical attention if they experience any of these symptoms.

Montelukast is contraindicated in individuals with known hypersensitivity to the drug or any of its excipients. Caution is also advised for patients with severe hepatic impairment, active psychiatric disorders, or those taking interacting medications without proper monitoring.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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