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

Montelukast Teva

Active Ingredient:
Montelukast Sodium
Origin:
EU

Montelukast Teva (Montelukast Sodium)

Montelukast, the active ingredient in Montelukast Teva, is a leukotriene receptor antagonist presented as an oral tablet for oral use. It is indicated for the maintenance treatment of asthma, for the prevention of exercise‑induced bronchoconstriction, and for relief of symptoms of seasonal 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, with capabilities for bulk manufacturing, quality assurance, and regulatory support across EU and other markets.

Manufacturer / TM Owner

Teva Nederland B.V.

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Indications & Clinical Uses

Montelukast is a leukotriene receptor antagonist used to manage conditions driven by leukotriene‑mediated airway inflammation.

  • Asthma: improves long‑term control and reduces frequency of exacerbations.
  • Exercise‑induced bronchoconstriction: prevents narrowing of airways during physical activity.
  • Allergic rhinitis: alleviates nasal congestion, sneezing and itching associated with seasonal allergies.

How It Works

  • Montelukast selectively blocks the cysteinyl leukotriene receptor CysLT1 on airway smooth‑muscle cells, mast cells and eosinophils. By antagonising the actions of leukotrienes D4, C4 and E4, it inhibits bronchoconstriction, vascular permeability and inflammatory cell recruitment, thereby reducing airway narrowing and mucosal edema associated with asthma and allergic rhinitis. The inhibition also dampens the release of pro‑inflammatory mediators, contributing to overall airway stability.

Side Effects

Montelukast is generally well tolerated, but several adverse reactions have been reported.

Common Side Effects

  • Headache: mild to moderate pain in the head.
  • Upper respiratory tract infection: sore throat, nasal congestion or cough.
  • Abdominal pain: discomfort or cramping in the stomach area.
  • Cough: occasional dry or productive cough.
  • Nausea: feeling of queasiness or urge to vomit.
  • Diarrhea: loose, watery stools.

Serious or Rare Side Effects

  • Neuropsychiatric events: agitation, depression, or suicidal thoughts.
  • Allergic reactions: rash, pruritus, angioedema, or anaphylaxis.
  • Hepatic dysfunction: elevated liver enzymes or jaundice.

Precautions & Warnings

Before prescribing Montelukast, clinicians should consider several safety and handling precautions.

  • Indication review: confirm diagnosis of asthma, exercise‑induced bronchoconstriction or allergic rhinitis before use.
  • Age considerations: safety data are limited in children under 12 months; use only as directed by a pediatric specialist.
  • Concomitant medications: assess for potential interactions, especially with phenobarbital or rifampin.
  • Monitoring: observe patients for new or worsening neuropsychiatric symptoms during therapy.
  • Pregnancy and lactation: evaluate risk‑benefit; limited data are available.
  • Store at ambient temperature: keep below 25 °C in the original container, protect from moisture and direct sunlight.

Avoid Interactions

Montelukast may interact with other medicines, altering its effectiveness or safety profile.

Major Interactions (Avoid)

  • Phenobarbital: enzyme induction may reduce montelukast plasma levels.
  • Rifampin: strong CYP3A4 inducer that can lower therapeutic exposure.
  • St. John’s wort: herbal CYP3A4 inducer potentially decreasing efficacy.

Moderate Interactions (Monitor Closely)

  • Antidepressants (SSRIs, SNRIs): may increase risk of neuropsychiatric side effects.
  • Warfarin: occasional reports of altered INR; monitor coagulation parameters.
  • Beta‑agonists: combined use may enhance bronchodilation but requires clinical assessment.

Frequently Asked Questions

Montelukast Teva contains the leukotriene receptor antagonist montelukast sodium and is prescribed for the long‑term management of asthma, the prevention of exercise‑induced bronchoconstriction, and the relief of symptoms associated with seasonal allergic rhinitis.

Montelukast blocks the cysteinyl leukotriene receptor CysLT1, preventing leukotrienes D4, C4 and E4 from triggering bronchoconstriction, airway swelling and inflammation, which helps keep the airways open and reduces allergic symptoms.

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

Safety data for montelukast in pregnancy and lactation are limited. Healthcare providers should weigh potential benefits against possible risks and discuss any concerns with the patient before initiating therapy.

To place an order, submit an enquiry on the Montelukast Teva 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 required import documentation.

Montelukast is an oral leukotriene receptor antagonist, offering an alternative to inhaled corticosteroids or long‑acting beta‑agonists for certain patients. It is particularly useful for those who prefer a once‑daily tablet or need additional control of exercise‑induced bronchoconstriction, but it is generally used as add‑on therapy rather than a sole replacement for inhaled steroids.

Montelukast tablets should be stored at ambient temperature, preferably below 25 °C, in the original blister pack or container. Keep the product away from moisture, direct sunlight and heat sources to maintain stability.

Montelukast Teva is taken orally, usually as a whole tablet swallowed with water. It is typically taken once daily in the evening, but patients should follow the specific timing advised by their prescriber.

Serious adverse reactions, although rare, include neuropsychiatric events such as agitation, depression or suicidal thoughts, severe allergic responses like anaphylaxis, and hepatic dysfunction manifested by elevated liver enzymes or jaundice. Patients should seek immediate medical attention if any of these symptoms occur.

Montelukast is contraindicated in individuals with known hypersensitivity to montelukast sodium or any of the tablet’s excipients. Caution is advised for patients with a history of severe neuropsychiatric disorders, liver disease, or those taking interacting enzyme‑inducing drugs without appropriate monitoring.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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