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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K31-7048
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filingDate 2000-06-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2004-03-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_642b7761819dd2e9e45f106f542ebd3c
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publicationDate 2004-03-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-1190720-B1
titleOfInvention Liquid pharmaceutical composition for oral administration of bitter hydrolysis-susceptible active substances
abstract Liquid pharmaceutical composition for the oral administration of active substances that are bitter and susceptible to hydrolysis. The composition (for 100 ml) comprises: 3-15 g of active substance; 0.01-0.3 g of preservative (sorbic acid, methyl p-hydroxybenzoate); sufficient amount of an edible oily vehicle formed by triglycerides of short- or medium-chain acids (caprylic, capric) to make up 100 ml; a suitable quantity of sweetener (sodium saccharin, sodium cyclamate, ammonium glycyrricinate) optionally accompanied by a suitable amount of a flavouring agent (walnut, condensed milk, coconut, banana); 0.5-2 g of soya lecithin; 0.1-5 g of thickener of the type derived from cellulose (N-ethylcellulose); and 0.05-1 g of a polysorbate type surfactant. Optionally it includes 0.5-5 g of mannitol and 1-5 g of sodium bicarbonate. It is useful for the administration of bitter active substances (ciprofloxacin, paracetamol, erythromycin etc.) in children, the elderly and patients who are little motivated. It is stable, easy to ingest and of bearable taste.
priorityDate 1999-06-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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