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FLUIMUCIL GRANULES 600MG/SACHET [SIN15144P]
Active ingredients: FLUIMUCIL GRANULES 600MG/SACHET
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Product Info
FLUIMUCIL GRANULES 600MG/SACHET
[SIN15144P]
Product information
Active Ingredient and Strength | ACETYLCYSTEINE - 600 MG |
Dosage Form | GRANULE, FOR SOLUTION |
Manufacturer and Country | ZAMBON SWITZERLAND LTD. - SWITZERLAND |
Registration Number | SIN15144P |
Licence Holder | UNITED ITALIAN TRADING CORPORATION (PRIVATE) LIMITED |
Forensic Classification | PHARMACY ONLY MEDICINES |
Anatomical Therapeutic Chemical (ATC) code | R05CB01 |
INDICATIONS
Fluimucil® A Effervescent Tablets 600mg and Fluimucil® Granules 600mg are indicated as an adjuvant treatment in certain clinical condition characterized by the presence of thick and viscous mucoid or mucopurulent secretions such as:
Chronic bronchopulmonary diseases (chronic obstructive pulmonary disease, emphysema with bronchitis, chronic asthmatic bronchitis, bronchiectasis);
Acute bronchopulmonary diseases (asthma with bronchial mucus plugging, bronchitis, bronchopneumonia, tracheobronchitis, bronchiolitis, pulmonary complications of cystic fibrosis, pulmonary complications associated with surgery).
POSOLOGY
Adults and children above 6 years
1 tablet of Fluimucil® A Effervescent Tablet 600 mg a day.
1 sachet of Fluimucil® Granules 600mg a day.
The duration of treatment should be 5 to 10 days in the acute treatment, whereas it may be continued in the chronic states for several months, according to the advice of the physician.
CONTRAINDICATIONS
Known hypersensitivity to acetylcysteine or to any of the excipients (please see below the section Warning and Precautions – please refer to the Product Insert/Patient Information Leaflet published on HSA for the full drug information).
Children under 2 years of age.
Fluimucil® A Effervescent Tablets 600mg and Fluimucil® Granules 600mg contain aspartame, thus it is contraindicated in patients suffering from phenylketonuria.
