• Asthma in Children Aged 2 to 14 Years Montelukast Sodium Chewable Tablet
  • Asthma in Children Aged 2 to 14 Years Montelukast Sodium Chewable Tablet
  • Asthma in Children Aged 2 to 14 Years Montelukast Sodium Chewable Tablet
  • Asthma in Children Aged 2 to 14 Years Montelukast Sodium Chewable Tablet
  • Asthma in Children Aged 2 to 14 Years Montelukast Sodium Chewable Tablet
  • Asthma in Children Aged 2 to 14 Years Montelukast Sodium Chewable Tablet

Asthma in Children Aged 2 to 14 Years Montelukast Sodium Chewable Tablet

MOQ: 100
Transport Package: Carton
Specification: 5mg 4mg
Trademark: Focus
Origin: China
Customization:
Gold Member Since 2021

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Rating: 5.0/5
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  • Overview
  • Product Parameters
  • Product Description
Overview

Basic Info.

Model NO.
Rhinitis and allergy
HS Code
3004909099
Production Capacity
100000000 Boxes/Month

Product Description

Product Parameters

 

Product name Montelukast Sodium Chewable Tablet
Main Ingredients Montelukast 
Adaptation disease The product is indicated for the prophylaxis and long-term treatment of asthma in children aged 2 to 14 years, including the prevention of daytime and nighttime asthma symptoms, the treatment of aspirin-sensitive asthma patients, and the prevention of exercise-induced bronchoconstriction.  This product is indicated for the relief of symptoms caused by allergic rhinitis (seasonal and perennial allergic rhinitis in children aged 2 to 14 years).  
Dosage form Troche
Character Pink piece
Specification (1)5mg  (2)4mg
Usage and dosage Once a day.  Asthma patients should take it before bed.  Allergic rhinitis patients can take medicine as needed according to their condition.  Patients with both asthma and allergic rhinitis should take the medicine once a night.  One tablet (5mg), once daily, in children 6 to 14 years of age with asthma and/or allergic rhinitis.  One tablet (4mg), once daily, in children 2 to 5 years of age with asthma and/or allergic rhinitis.  It is generally recommended that asthma control indicators be used to evaluate the therapeutic effect, and the efficacy of this product appears within one day of administration.  This product can be taken with food or in addition.  Patients should be advised to continue taking asthma during periods of control and progression.  There is no need to adjust the dose for patients with renal insufficiency, patients with mild to moderate liver damage, and patients of different genders.  Relationship with other asthma medications This product can be added to the patient's existing treatment regimen.  Reduce the dose of combined drugs: bronchodilators for asthma patients who cannot be effectively controlled by bronchodilators alone, this product can be added to the treatment plan. Once there is a clinical treatment response (generally after the first dose of medication), the dose of bronchodilators can be reduced according to the patient's tolerance.  Inhaled glucocorticoid for asthma patients receiving inhaled glucocorticoid treatment after the addition of this product, according to the patient's tolerance can be appropriately reduced dose.  Should be gradually reduced under the guidance of doctors.  In some patients, inhaled corticosteroids may be gradually reduced until they are completely discontinued.  However, this product should not be used as a sudden replacement for inhaled corticosteroids or on medical advice.  
Storage Keep away from light, sealed, in a cool (not more than 20 ºC) dry place
Origin China
validity 24 months
Tatoo Allergic to any of the ingredients in this product is not allowed.
Notice 1. The efficacy of oral administration in the treatment of acute asthma attacks has not been determined.  Therefore, it should not be used to treat acute asthma attacks.  Patients should be informed to prepare appropriate salvage medications. 
Sudden substitution of inhaled or oral glucocorticoids should not be used, although the combined dose of inhaled corticosteroids may be gradually reduced under the guidance of a physician. 
Neuropsychiatric events have been reported in patients taking this product (see adverse reactions).  As other factors may also cause these events, they cannot be confirmed to be related to this product.  Physicians should discuss these adverse events with patients and/or caregivers.  The patient and/or caregiver should be informed and the doctor should be notified if these conditions occur. 
Patients treated with antiasthmatic medications, including leukotriene receptor antagonists, rarely develop one or more of the following conditions: acidic granulocytosis, vascular rash, worsening of pulmonary symptoms, cardiac complications, and/or neuropathy (sometimes diagnosed as churg-Strauss syndrome, a systemic eosinophilic vasculitis).  These conditions are sometimes associated with reduction or discontinuation of oral glucocorticoid therapy.  Although the causal relationship between these conditions and leukotriene receptor antagonists has not been established, attention and appropriate clinical monitoring are recommended for patients taking singulair. 
2. Medication for pregnant and lactating women 
Pregnant women should avoid taking this product unless explicitly required. 
Global post-marketing experience has shown that rare neonatal congenital limb defects have been reported after use of this product during pregnancy.  The vast majority of these women also used other asthma medications during pregnancy.  A causal relationship between the use of this product and these events has not been established. 
It is not clear whether this product can be secreted from breast milk.  Since many drugs can be secreted from breast milk, lactating women should use this product with caution. 
3. Medication for children 
Safety and efficacy studies have been conducted in children aged 6 months to 14 years.  For children aged 2 to 14 years, please refer to montelukast sodium chewable tablets [Usage and dosage].  Safety and efficacy in children younger than 6 months have not been studied.  Studies have shown that this product does not affect the growth rate of children.  Special patient 
4. There is no need to adjust the dose for the elderly, patients with renal insufficiency or patients with mild to moderate hepatic insufficiency.  There was no clinical data for montelukast in patients with severe liver insufficiency (Child-pugh score >9).  
Product Description

 

Asthma in Children Aged 2 to 14 Years Montelukast Sodium Chewable TabletAsthma in Children Aged 2 to 14 Years Montelukast Sodium Chewable Tablet

It is available in pink tablets, 5 mg round pink tablets, 4 mg oval pink tablets.  
 

This product is suitable for the age of 2 to 14 years old of children asthma prevention and treatment for a long time, including the prevention of asthma symptoms of day and night, sensitive to aspirin treatment of patients with asthma and prevent exercise induced bronchoconstriction, can also reduce allergic rhinitis symptoms caused (2 years old to 14 years old children of seasonal allergic rhinitis and perennial allergic rhinitis)  
 

This product is packed with aluminum plastic board, we can provide two kinds of packaging:  

(1) 5mg, 5 tablets/box, 6 tablets/box, 7 tablets/box, 7 tablets ×2 tablets/box, 12 tablets/box,18 tablets/box,24 tablets/box  

(2) 4mg, 5 tablets/box, 6 tablets/box, 7 tablets/box, 7 tablets ×2 tablets/box, 12 tablets/box,18 tablets/box,24 tablets/box  
 

Please refer to the above table for usage and precautions.  

To get more information, just feel free to contact with us.  Thanks. 
 
 

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Gold Member Since 2021

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Rating: 5.0/5
Trading Company
Registered Capital
10800000 RMB
Plant Area
101~500 square meters