http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-2026766-A1

Outgoing Links

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_0a4783407e23a20dbe43d383a5d0fcb5
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K9-2027
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K9-2054
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K9-20
filingDate 2007-05-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7832fe628a4d4166e1f96e8211e791bb
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ae511abed59b7ad823b56ed9292b75e1
publicationDate 2009-02-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-2026766-A1
titleOfInvention Tablet composition with a prolonged release of tamsulosin
abstract The invention relates to a controlled release pharmaceutical tablet comprising: a) 0.1 to 1 weight % of tamsulosin, preferably tamsulosin hydrochloride; b) 40-80 weight % of a water-swellable matrix-forming composition comprising (i) a pH- sensitive swellable hydrophilic polymer, which is a cross-linked polyacrylic acid polymer, and (ii) a pH-insensitive swellable hydrophilic polymer; and c) optionally a water insoluble binder.
priorityDate 2006-05-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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