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 formulation for oral use. It treats asthma, exercise‑induced bronchoconstriction and allergic rhinitis 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 Sweden Ab

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Indications & Clinical Uses

Montelukast Teva is a leukotriene receptor antagonist used in respiratory and allergic disorders.

  • Asthma: improves control of chronic asthma and reduces the frequency of exacerbations.
  • Exercise‑induced bronchoconstriction: prevents airway narrowing that occurs during physical activity.
  • Allergic rhinitis: alleviates nasal congestion, sneezing and itching caused by seasonal allergies.

How It Works

  • Montelukast selectively blocks the cysteinyl leukotriene receptor CysLT1, preventing leukotrienes D4, C4 and E4 from binding. This inhibition reduces bronchoconstriction, vascular permeability and inflammatory cell recruitment in the airways, thereby improving airflow and decreasing allergic inflammation.

Side Effects

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

Common Side Effects

  • Headache: mild to moderate pain in the head.
  • Abdominal pain: discomfort or cramps in the stomach area.
  • Nausea: feeling of queasiness or urge to vomit.
  • Dizziness: sensation of light‑headedness or unsteadiness.
  • Fatigue: unusual tiredness or lack of energy.
  • Cough: transient irritation of the throat.

Serious or Rare Side Effects

  • Allergic reactions: rash, angioedema or anaphylaxis.
  • Neuropsychiatric events: mood changes, depression or suicidal thoughts.
  • Hepatic enzyme elevation: abnormal liver function tests.
  • Eosinophilic granulomatosis with polyangiitis: rare vasculitic disorder.
  • Stevens‑Johnson syndrome: severe skin and mucous membrane reaction.
  • Blood dyscrasias: rare cases of neutropenia or thrombocytopenia.

Precautions & Warnings

Before initiating therapy, clinicians should consider several safety aspects.

  • Liver function assessment: evaluate hepatic status, especially in patients with known liver disease.
  • Neuropsychiatric monitoring: watch for mood changes, depression or suicidal ideation.
  • Hypersensitivity: avoid in individuals with known allergy to montelukast or any tablet excipients.
  • Pediatric dosing: follow age‑specific recommendations provided by the prescriber.
  • Drug interactions: review concomitant medications that may affect montelukast metabolism.
  • Store at below 25°C: keep in the original packaging, protect from moisture and direct sunlight.

Avoid Interactions

Montelukast may interact with other medicines that influence its metabolism or pharmacodynamic profile.

Major Interactions (Avoid)

  • Strong CYP3A4 inhibitors (e.g., ketoconazole, itraconazole): may increase montelukast plasma concentrations.
  • Rifampin or other potent CYP inducers: may markedly reduce therapeutic effect.
  • Phenobarbital: can lower montelukast levels, compromising efficacy.

Moderate Interactions (Monitor Closely)

  • Warfarin: occasional reports of altered INR; monitor coagulation parameters.
  • Phenylephrine or pseudoephedrine: may increase risk of cardiovascular side effects.
  • Theophylline: monitor for additive bronchospastic effects.
  • Antidepressants (SSRIs): observe for enhanced neuropsychiatric symptoms.

Frequently Asked Questions

Montelukast Teva is prescribed for the long‑term management of asthma, to prevent exercise‑induced bronchoconstriction, and to relieve symptoms of allergic rhinitis such as nasal congestion, sneezing and itching.

Montelukast Sodium blocks the cysteinyl leukotriene receptor CysLT1, preventing leukotrienes D4, C4 and E4 from triggering bronchoconstriction, airway swelling and mucus production, thereby improving breathing and reducing allergic inflammation.

The appropriate dose of Montelukast Teva is determined by the prescribing healthcare professional based on the patient’s age, condition and response to therapy. Patients should follow the prescriber’s instructions and not adjust the dose on their own.

Safety data for Montelukast during pregnancy and lactation are limited. Healthcare providers should weigh the potential benefits against possible risks and discuss any concerns with the patient before prescribing.

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 or long‑acting beta‑agonists. It is particularly useful for patients who need add‑on therapy, have exercise‑induced symptoms, or prefer a non‑inhaled option.

Montelukast Teva should be stored at temperatures below 25 °C, in its original packaging, protected from moisture and direct sunlight. Do not store in a bathroom or near heat sources.

Montelukast Teva is taken orally, usually once daily, with or without food. The tablet should be swallowed whole with a glass of water; it should not be crushed, chewed, or split unless specifically instructed by a healthcare professional.

Serious risks include rare allergic reactions such as rash, angioedema or anaphylaxis, and neuropsychiatric events like mood changes, depression or suicidal thoughts. Patients should seek immediate medical attention if any of these symptoms occur.

Montelukast Teva should be avoided in individuals with known hypersensitivity to montelukast sodium or any of the tablet’s excipients. It is also contraindicated in patients who have experienced severe allergic reactions to the drug in the past.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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