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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P3-10
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P3-08
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-425
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filingDate 1991-10-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_80548ab4a6277626d3aa47b14f098215
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_673121aaeb2ef60b15b215fcd2720090
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publicationDate 1993-04-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H0597670-A
titleOfInvention Preparation for oral administration
abstract (57) [Summary] [Structure] General formula (However, R is a phenyl group or naphthyl group which may have a substituent, and Alk is a lower alkylene group.) As an active ingredient, an ultrafine powder of a benzoxazole derivative or a pharmaceutically acceptable salt thereof is used. A formulation for oral administration containing. [Effect] It has a stable and high bioavailability for effectively exerting the drug effect of the above-mentioned benzoxazole derivative, and is excellent as an oral administration preparation for treating diabetes.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2005105109-A1
priorityDate 1991-10-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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