Product image of Montelukast Bristol Laboratories (Montelukast Sodium) supplied by GNH India

Montelukast Bristol Laboratories

Active Ingredient:
Montelukast Sodium
Origin:
EU

Montelukast Bristol Laboratories (Montelukast Sodium)

Montelukast, the active ingredient in Montelukast Bristol Laboratories, is a leukotriene receptor antagonist presented as an oral tablet for oral use. It helps control symptoms of asthma, allergic rhinitis and exercise‑induced bronchoconstriction in adults and children.
GNH India supplies Montelukast Bristol Laboratories as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Bristol Laboratories Limited

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Indications & Clinical Uses

  • Montelukast is a leukotriene receptor antagonist used to manage conditions driven by cysteinyl leukotriene activity.
  • Asthma: improves long‑term control and reduces the frequency of asthma attacks.
  • Allergic rhinitis: alleviates nasal congestion, sneezing and itching caused by seasonal or perennial allergens.
  • Exercise‑induced bronchoconstriction: prevents airway narrowing that occurs during or after physical exertion.

How It Works

  • Montelukast selectively blocks the cysteinyl leukotriene receptor CysLT1, preventing leukotriene D4 and related mediators from binding. This inhibition reduces bronchoconstriction, vascular permeability, mucus secretion, and inflammatory cell recruitment in the airways, thereby improving respiratory function and reducing allergic inflammation.

Side Effects

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

Common Side Effects

  • Headache: mild to moderate intensity.
  • Abdominal pain or dyspepsia.
  • Cough or throat irritation.
  • Nasal congestion or rhinorrhea.
  • Fatigue or somnolence.
  • Mild rash or itching.

Serious or Rare Side Effects

  • Allergic reactions: urticaria, angioedema, anaphylaxis.
  • Neuropsychiatric events: agitation, depression, suicidal thoughts.
  • Hepatotoxicity: elevated liver enzymes, hepatitis.
  • Stevens‑Johnson syndrome or toxic epidermal necrolysis.
  • Severe bronchospasm in rare cases.
  • Blood dyscrasias: eosinophilia, neutropenia.

Precautions & Warnings

  • When prescribing Montelukast, clinicians should consider several safety aspects.
  • Monitor neuropsychiatric symptoms: watch for mood changes, depression, or suicidal ideation.
  • Assess hepatic function: use caution in patients with liver impairment.
  • Avoid use in acute asthma attacks: not a rescue medication.
  • Check for hypersensitivity: discontinue if allergic reaction occurs.
  • Pregnancy and lactation: only if benefit outweighs risk.
  • Store below 25°C: keep in the original packaging, protect from moisture and direct sunlight.

Avoid Interactions

Montelukast may interact with other medicines, requiring attention to co‑administration.

Major Interactions (Avoid)

  • Strong CYP3A4 inhibitors (e.g., ketoconazole, itraconazole): may increase montelukast levels.
  • Phenobarbital or rifampicin: potent inducers that can reduce efficacy.

Moderate Interactions (Monitor Closely)

  • Warfarin: potential alteration of anticoagulant effect.
  • Other leukotriene modifiers (e.g., zafirlukast): additive pharmacologic effect.
  • Fluconazole: may modestly increase exposure.
  • Antidepressants: monitor for enhanced neuropsychiatric side effects.

Frequently Asked Questions

Montelukast Bristol Laboratories is indicated for the long‑term management of asthma, relief of symptoms associated with allergic rhinitis, and prevention of exercise‑induced bronchoconstriction. It works by blocking leukotriene receptors that contribute to airway inflammation and constriction.

Montelukast selectively antagonizes the cysteinyl leukotriene receptor CysLT1, preventing leukotriene D4 and related mediators from binding. This blockade reduces bronchoconstriction, mucus production, and inflammatory cell recruitment, helping to keep the airways open and less reactive.

The dosage of Montelukast is determined by the prescribing clinician based on the patient’s age, weight, and specific condition. It is typically taken once daily in the evening, but exact dosing instructions must be obtained from a qualified healthcare professional.

Safety data for Montelukast in pregnancy and lactation are limited. It should only be used if the potential benefit justifies any possible risk to the fetus or infant, and the decision must be made by the prescriber in consultation with the patient.

To place an order, 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 and long‑acting beta‑agonists. It is particularly useful for patients with allergic components or exercise‑induced symptoms, but it does not replace rescue bronchodilators for acute attacks.

Montelukast tablets should be stored below 25 °C in a dry place. Keep them in the original container, protect from moisture and direct sunlight, and ensure they are out of reach of children.

Montelukast is taken orally, usually as a tablet swallowed whole with water. It is generally recommended to take the dose in the evening, but patients should follow the specific instructions provided by their healthcare provider.

Serious risks include rare but severe allergic reactions such as anaphylaxis, neuropsychiatric events like depression or suicidal thoughts, and liver injury. Patients should seek immediate medical attention if they experience any signs of these conditions.

Montelukast is contraindicated in individuals with known hypersensitivity to the drug or any of its components. It should not be used as a rescue medication for acute asthma attacks, and patients with severe liver disease should use it only under close medical supervision.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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