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

Montelukast Unimark

Active Ingredient:
Montelukast Sodium
Origin:
EU

Montelukast Unimark (Montelukast Sodium)

Montelukast, the active ingredient in Montelukast Unimark, is a leukotriene receptor antagonist presented as an oral dosage form for systemic use. It is employed to manage asthma and allergic rhinitis in adult and pediatric patients.

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

Manufacturer / TM Owner

Unimark Remedies Sro

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Indications & Clinical Uses

Montelukast acts on the leukotriene pathway to control chronic airway diseases.

  • Asthma: improves long‑term control and reduces exacerbations.
  • Allergic rhinitis: alleviates nasal congestion, sneezing and itching.
  • Exercise‑induced bronchoconstriction: prevents airway narrowing triggered by physical activity.

How It Works

  • Montelukast selectively blocks the cysteinyl leukotriene receptor CysLT1, preventing leukotriene D4 from binding. This inhibition reduces leukotriene‑mediated bronchoconstriction, vascular permeability, and inflammatory cell recruitment, thereby improving airway patency and decreasing allergic inflammation.

Side Effects

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

Common Side Effects

  • Headache: mild to moderate intensity.
  • Abdominal pain: occasional discomfort.
  • Cough: transient respiratory irritation.
  • Nausea: occasional upset stomach.
  • Diarrhea: loose stools.
  • Upper respiratory infection: mild cold‑like symptoms.

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.
  • Stevens‑Johnson syndrome: severe skin eruption.
  • Eosinophilic pneumonia: rare lung inflammation.
  • Severe hypersensitivity: bronchospasm or anaphylactoid response.

Precautions & Warnings

Before initiating therapy, clinicians should consider several safety aspects.

  • Assess asthma control: ensure baseline therapy is optimized.
  • Monitor neuropsychiatric symptoms: watch for mood changes or suicidal ideation.
  • Avoid in patients with known hypersensitivity to montelukast or excipients.
  • Use caution in hepatic impairment: dose adjustment may be required.
  • Review concomitant medications for potential interactions.
  • Store at ambient temperature below 25°C: keep in original packaging, protect from moisture and direct sunlight.

Avoid Interactions

Montelukast may interact with other medicines, influencing its efficacy or safety.

Major Interactions (Avoid)

  • Strong CYP3A4 inhibitors (e.g., ketoconazole, itraconazole): may increase montelukast plasma levels.
  • Potent CYP2C9 inhibitors (e.g., fluconazole): could raise exposure.
  • Phenobarbital or rifampicin: enzyme inducers that markedly reduce effectiveness.

Moderate Interactions (Monitor Closely)

  • Warfarin: possible alteration of anticoagulant effect.
  • Ritonavir: may modestly increase montelukast concentrations.
  • Other leukotriene modifiers: additive effects on leukotriene pathways.
  • Antidepressants (e.g., fluoxetine): monitor for neuropsychiatric signs.
  • Beta‑agonists: no direct interaction but combined therapy may affect symptom control.

Frequently Asked Questions

Montelukast Unimark is indicated for the long‑term management of asthma, the relief of symptoms associated with allergic rhinitis, and the prevention of exercise‑induced bronchoconstriction. It helps reduce airway inflammation and improve breathing in patients with these respiratory conditions.

Montelukast selectively blocks the cysteinyl leukotriene receptor CysLT1, preventing leukotriene D4 from binding. This action stops leukotriene‑driven bronchoconstriction, mucus production, and inflammatory cell recruitment, thereby easing airway narrowing and allergic inflammation.

The appropriate dose of Montelukast Unimark is determined by the prescribing healthcare professional based on the patient’s age, weight, and specific indication. Dosage regimens are individualized and should follow the prescriber’s instructions.

Safety data for Montelukast in pregnancy and lactation are limited. Healthcare providers should weigh the potential benefits against any possible risks before prescribing to pregnant or nursing women, and discuss alternative options when appropriate.

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 with aspirin‑exacerbated respiratory disease or those who prefer a once‑daily oral tablet, though it is generally used as add‑on therapy rather than a sole controller.

Montelukast Unimark should be stored at ambient temperature below 25 °C. Keep the product in its original packaging, protect it from moisture and direct sunlight, and ensure the container is tightly closed to maintain stability.

Montelukast Unimark is taken orally, usually once daily in the evening, with or without food. The tablet should be swallowed whole with a glass of water and not chewed or crushed unless otherwise directed by a healthcare professional.

Serious risks include rare but severe allergic reactions such as rash, angioedema, or anaphylaxis, as well as neuropsychiatric events like mood changes, depression, or suicidal thoughts. Patients should be monitored closely for any unusual symptoms and seek immediate medical attention if they occur.

Montelukast Unimark is contraindicated in individuals with known hypersensitivity to montelukast sodium or any of the tablet’s excipients. It should also be used with caution in patients with severe hepatic impairment or those taking interacting medications that could alter its effectiveness.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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