Mucosolvan

Country: Malta

Language: English

Source: Medicines Authority

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Active ingredient:

AMBROXOL HYDROCHLORIDE

Available from:

Boehringer Ingelheim Ellas A.E. Ellinikou 2, 167 77 Elliniko, Athens, Greece

ATC code:

R05CB06

INN (International Name):

AMBROXOL HYDROCHLORIDE 15 mg/5ml

Pharmaceutical form:

SYRUP

Composition:

AMBROXOL HYDROCHLORIDE 15 mg/5ml

Prescription type:

POM

Therapeutic area:

COUGH AND COLD PREPARATIONS

Authorization status:

Withdrawn

Authorization date:

2006-08-30

Patient Information leaflet

                                1.
SPECIFICATION OF THE MEDICINAL PRODUCT
1.1 NAME OF THE MEDICINAL PRODUCT: MUCOSOLVAN
1.2 COMPOSITION:
TABLETS: Active ingredient: Ambroxol Hydrochloride
Excipients: Lactose monohydrate, Starch maize, Silicon dioxide
colloidal,
Magnesium Stearate.
SYRUP: Active ingredient: Ambroxol Hydrochloride
Excipients: Hydroxyethylcellulose, Sorbitol solution 70%, Glycerol
85%,
Benzoic acid, Raspberry flavour D 9599, Propylene glycol, Tartaric
acid,
Purified water
1.3 PHARMACEUTICAL FORM:
Tablets, Syrup
1.4 QUANTITY OF ACTIVE INGREDIENT:
Each tablet contains 30mg trans-4-[(2-amino-3,5 dibromobenzyl) amino]
cyclohexanol  hydrochloride (=Ambroxol hydrochloride )
5ml of syrup contain 15mg   trans-4-[(2-amino-3,5-dibromobenzyl)
amino] cyclohexanol hydrochloride (=Ambroxol hydrochloride )
1.5 DESCRIPTION AND PACKAGING:
TABLETS: White with score, imprinted with code 67C and company logo,
diameter approximately 9 mm. Tablets 30mg in a box of 20.
SYRUP: Clear or almost clear, colourless slightly viscous syrup.
Syrup in a
glass bottle of 125 ml.  
1.6 PHARMACOTHERAPEUTIC GROUP:
Mucolytic, improves mucus transportation.
1.7 RESPONSIBLE FOR PLACING THE PRODUCT IN THE MARKET :
Boehringer Ingelheim Ellas Α.Ε
Ellinikou 2
167 77 Elliniko (Athens)
Tel.: +30 210 89 06 111
1.8 MANUFACTURER:
Boehringer Ingelheim Ellas Α.Ε.
Koropi, Attika, Greece
1.9 PACKAGER:
Boehringer Ingelheim Ellas Α.Ε.
Koropi, Attika, Greece.
2.  WHAT YOU SHOULD KNOW ABOUTTHE MEDICINE YOUR DOCTOR 
PRESCRIBED TO YOU
The information provided by this leaflet is only for this
particular medicine.
Please read this leaflet carefully. Because this leaflet does not
contain the
complete information about your medicine, if you have any questions
or
you are not sure about something,
ask your doctor or your pharmacist. 
2.1 GENERAL INFORMATION:
Mucosolvan improves mucus transportation (stimulates
ciliarry activity
and as a result enhances mucus clearance) and has secretolytic
properties.
It facilitates the removal of tracheob
                                
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Summary of Product characteristics

                                Page 1 of 4 
SUMMARY OF PRODUCT CHARACTERISTICS 
 
 
 
1. .  NAME OF THE MEDICINAL PRODUCT 
 
   MUCOSOLVAN
®
 
 
 
2. QUALITATIVE AND QUANTITATIVE COMPOSITION 
 
   trans-4-[(2-amino-3,5-dibromobenzyl) amino] cyclohexanol
hydrochloride 
   (=Ambroxol hydrochloride ) 
 
   5 ml Syr = 15 mg  
 
   For excipients see 6.1 
 
 
3. PHARMACEUTICAL FORM 
 
     Syrup 
 
 
4. CLINICAL PARTICULARS 
 
4.1.  THERAPEUTIC INDICATIONS 
As adjuvant for the fluidization of the mucus secretions of the
respiratory tract in cases of 
acute and chronic bronchopulmonary diseases (bronchitis, emphysema,
tracheobronchitis, 
chronic asthmatic bronchitis).   
Also is indicated for the prevention of respiratory complications
after surgical operations 
of the chest.  
During acute exacerbations of bronchitis must be administrated as
concomitant therapy 
with the appropriate antibiotic.  
 
4.2.     POSOLOGY AND METHOD OF ADMINISTRATION 
         For children is recommended as total daily dose 1.2-1.6
mg/kg body weight. 
If there are not other instructions
:
  
Children 5-12 years
:
 1 tea spoon 2-3 times daily. 
Children 2-5 years
:
 1/2 tea spoon 3 times daily. 
Children below 2 years
:
 1/2 tea spoon 2 times daily. 
 
The above mentioned dose is indicated in acute conditions of the
respiratory system and 
for the initiation of the treatment of chronic conditions, and can
be continued for a period 
of 10 days. If the treatment must be continued for more than ten
days the dose must be 
reduced to the half.      
 
4.3.   CONTRAINDICATIONS  
         Not to be used during pregnancy and lactation. 
Mucosolvan should not be used in patients known to be hypersensitive
to ambroxol or 
other components of the formulation. 
Page 2 of 4 
 
4.4.     SPECIAL WARNINGS AND SPECIAL PRECAUTIONS FOR USE 
During administration can provoke increase of the fluidizated mucus
secretions and if they 
are not removed by
                                
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