Montair-ODT
Generic Name
Montelukast
Manufacturer
Cipla Ltd.
Country
India
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Price Details
Current market pricing information
| Variant | Unit Price | Strip Price |
|---|---|---|
| montair odt 4 mg tablet | ৳ 7.00 | ৳ 70.00 |
Description
Overview of the medicine
Montair-ODT 4 mg Tablet is an orally disintegrating tablet containing Montelukast, used for the prevention and long-term treatment of asthma and for the relief of symptoms of seasonal allergic rhinitis, especially in pediatric patients aged 2 to 5 years. The ODT formulation allows for easy administration without water.
Uses & Indications
Dosage
Adults
Not typically used for adults. Adult dosage for Montelukast is usually 10 mg once daily.
Elderly
Not typically used for elderly. Elderly dosage for Montelukast is usually 10 mg once daily.
Renal_impairment
No dosage adjustment is required for patients with renal impairment.
Children_2_5_years
One 4 mg orally disintegrating tablet daily in the evening. Tablets should not be opened until ready to use. After opening the sachet, the entire tablet should be placed directly on the tongue, where it rapidly disintegrates and can be swallowed with saliva. No water is needed. For asthma, the dose should be taken in the evening. For allergic rhinitis, the time of administration may be individualized to suit patient needs. Patients with both asthma and allergic rhinitis should take one dose in the evening.
Hepatic_impairment
No dosage adjustment is required for patients with mild to moderate hepatic impairment. No clinical studies in patients with severe hepatic impairment.
How to Take
Montair-ODT 4 mg tablet is an orally disintegrating tablet. Do not open the sachet until you are ready to use it. Once opened, place the entire tablet directly on your tongue. It will rapidly disintegrate and can be swallowed with your saliva. No water is needed. Take it once daily in the evening, with or without food.
Mechanism of Action
Montelukast is a selective and orally active leukotriene receptor antagonist that specifically inhibits the cysteinyl leukotriene CysLT1 receptor. Cysteinyl leukotrienes (LTC4, LTD4, LTE4) are potent inflammatory eicosanoids released from various cells, including mast cells and eosinophils, and are associated with the pathophysiology of asthma and allergic rhinitis. By blocking these receptors, montelukast inhibits bronchoconstriction, mucus secretion, vascular permeability, and eosinophil recruitment, thereby reducing inflammation and improving respiratory function.
Pharmacokinetics
Onset
Clinical effects may be seen within one day of administration for asthma and allergic rhinitis symptoms.
Excretion
Excreted almost exclusively via bile in feces. Less than 0.2% is excreted in urine.
Half life
Plasma half-life ranges from 2.7 to 5.5 hours in healthy adults.
Absorption
Rapidly absorbed after oral administration. Mean peak plasma concentration (Tmax) is approximately 2 hours for the 4 mg ODT in children aged 2 to 5 years. Bioavailability is generally good.
Metabolism
Extensively metabolized in the liver, primarily by CYP2C8, with minor contributions from CYP3A4 and CYP2C9. Metabolites are pharmacologically inactive.
Side Effects
Contraindications
- •Hypersensitivity to Montelukast or any component of the formulation.
- •Acute asthma attacks (not indicated for reversal of bronchospasm in acute asthma).
Drug Interactions
Rifampicin
May decrease montelukast plasma levels. Monitor clinical response.
Phenobarbital
May decrease the area under the plasma concentration-time curve (AUC) of montelukast by approximately 40%.
Storage
Store below 30°C (86°F) in a dry place, protected from light and moisture. Keep out of reach of children.
Overdose
In post-marketing experience, there have been reports of acute overdose with montelukast. The most frequently reported adverse events were abdominal pain, somnolence, thirst, headache, vomiting, and psychomotor hyperactivity. Treatment is symptomatic and supportive. It is not known if montelukast is dialyzable by peritoneal or hemodialysis.
Pregnancy & Lactation
Pregnancy Category B. Studies in animals have shown no evidence of harm to the fetus. There are no adequate and well-controlled studies in pregnant women. Use during pregnancy only if clearly needed. It is unknown whether montelukast is excreted in human milk. Exercise caution when administering to a nursing mother.
Frequently Asked Questions
Common questions about this medicine
Pack Sizes
Shelf Life
Typically 24-36 months from the date of manufacture. Refer to the packaging for the exact expiry date.
Availability
Available in pharmacies nationwide
Approval Status
Approved by major regulatory bodies (e.g., FDA, DGDA)
Patent Status
Patent expired for generic versions
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