Product image of Modulair (Montelukast) supplied by GNH India

Modulair

Active Ingredient:
Montelukast
Origin:
EU

Modulair (Montelukast)

Montelukast, the active ingredient in Modulair, is a leukotriene receptor antagonist presented as a tablet for oral use. It is indicated for asthma maintenance therapy, allergic rhinitis, and exercise‑induced bronchoconstriction in adults and children.
GNH India supplies Modulair as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Elpen Pharmaceutical Co. Inc.

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Indications & Clinical Uses

Montelukast acts on the leukotriene pathway to control chronic respiratory conditions.

  • Asthma maintenance therapy: reduces the frequency and severity of asthma symptoms and exacerbations.
  • Allergic rhinitis: alleviates nasal congestion, sneezing, and itching caused by seasonal or perennial allergens.
  • Exercise‑induced bronchoconstriction: prevents airway narrowing during physical activity, improving exercise tolerance.

How It Works

  • Montelukast selectively blocks the cysteinyl leukotriene receptor CysLT1, preventing leukotrienes from binding and triggering bronchoconstriction, mucus secretion, and airway inflammation. By inhibiting this pathway, the drug reduces airway hyper‑responsiveness and inflammatory cell recruitment, contributing to improved respiratory function in asthma and allergic conditions.

Side Effects

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

Common Side Effects

  • Headache: mild to moderate pain often reported during treatment.
  • Abdominal pain: discomfort or cramps in the stomach area.
  • Nausea: feeling of queasiness without vomiting.
  • Dizziness: transient light‑headedness or balance disturbance.

Serious or Rare Side Effects

  • Allergic reactions: including angioedema, urticaria, or anaphylaxis.
  • Neuropsychiatric events: mood changes, agitation, or suicidal thoughts.
  • Hepatic enzyme elevation: abnormal liver function tests.
  • Severe skin reactions: such as Stevens‑Johnson syndrome or toxic epidermal necrolysis.

Precautions & Warnings

Before initiating therapy, clinicians should consider several safety aspects.

  • Liver function assessment: evaluate hepatic status, especially in patients with pre‑existing liver disease.
  • Neuropsychiatric monitoring: watch for mood alterations, depression, or suicidal ideation.
  • Severe asthma caution: do not substitute for rescue inhalers in acute attacks.
  • Hypersensitivity check: avoid use in individuals with known allergy to montelukast or any tablet excipients.
  • Store below 25°C: keep in the original pack, protect from moisture.

Avoid Interactions

Montelukast may interact with other medicines, requiring attention to potential changes in efficacy or safety.

Major Interactions (Avoid)

  • Strong CYP3A4 inducers (e.g., rifampin, carbamazepine): may markedly reduce montelukast plasma levels.
  • Phenobarbital: can lower drug exposure, compromising therapeutic effect.

Moderate Interactions (Monitor Closely)

  • Selective serotonin reuptake inhibitors (e.g., fluoxetine, sertraline): may increase risk of neuropsychiatric side effects.
  • ACE inhibitors (e.g., lisinopril): combined use may raise the chance of angioedema.
  • Theophylline: additive bronchodilator effect may require dose adjustment.

Frequently Asked Questions

Modulair contains montelukast, which is prescribed for asthma maintenance therapy, allergic rhinitis, and exercise‑induced bronchoconstriction. It helps control chronic airway inflammation and prevents symptoms triggered by allergens or physical activity.

Montelukast blocks the cysteinyl leukotriene receptor CysLT1, stopping leukotrienes from causing bronchoconstriction, mucus production, and inflammation. By inhibiting this pathway, the drug reduces airway narrowing and allergic responses.

The specific dose of Modulair is determined by the prescribing clinician based on the patient’s age, weight, and clinical condition. Healthcare providers set the appropriate regimen according to approved guidelines.

Safety data for montelukast in pregnancy are limited, and the product is classified as pregnancy category unknown. It should be used only if the potential benefit justifies any potential risk. Caution is also advised during breastfeeding, and a healthcare professional should evaluate the risk‑benefit balance.

To request Modulair, 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.

Modulair (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 who prefer oral therapy or need additional control of allergic components, but it does not replace rescue inhalers for acute attacks.

Modulair tablets should be stored below 25 °C, in the original packaging, and protected from moisture. Avoid exposure to high humidity or direct sunlight to maintain product stability.

Modulair is taken orally, usually once daily in the evening, with or without food, as directed by a healthcare professional. Swallow the tablet whole; do not crush or chew it.

Serious risks include severe allergic reactions such as angioedema or anaphylaxis, neuropsychiatric events like mood changes or suicidal thoughts, and rare skin conditions such as Stevens‑Johnson syndrome. Patients should seek immediate medical attention if any of these occur.

Modulair should be avoided in individuals with known hypersensitivity to montelukast or any tablet excipients. It is also not suitable as a rescue medication for acute asthma attacks and should be used with caution in patients with severe liver impairment.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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