http://rdf.ncbi.nlm.nih.gov/pubchem/patent/TW-200425914-A

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K45-08
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P9-06
filingDate 2001-08-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_451af8628f6dd07add8b88e09fa7c945
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_20938f9638915bab612f5b39a57be49c
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_150d87d5ea3dd97f97d7f15f03ea99ab
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_412071e62f8841e653ec4363694a5725
publicationDate 2004-12-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber TW-200425914-A
titleOfInvention Pharmaceutical tablet composition comprising n-[(1-nbutyl-4-piperidinyl)methyl]-3,4-dihydro-2h-[1,3]oxazino[3,2-a]indole-10-carboxamide (sb 207266) or a salt thereof
abstract The present invention relates to a pharmaceutical composition being a tablet for human oral administration, comprising N-[(1-nbutyl-4-piperidinyl)methyl]-3,4-dihydro-2H-[1,3]oxazino[3,2-a]indole-10-carboxa mide (SB 207266) or a pharmaceutically acceptable salt thereof in combination with a pharmaceutically acceptable solid carrier, wherein the SB 207266 or the salt thereof is present in the tablet in at least 5.0 mg per 250 mg of tablet weight (measured as the free base), wherein the tablet is the result of a granulation process, and wherein the composition includes dicalcium phosphate. Preferably, the composition is substantially as follows, provided that the dose of the SB-207266 in the composition can be increased: SB-207266 5.0 mg Microcrystalline cellulose 50.0 mg Hydroxypropylmethylcellulose (HPMC) 12.5 mg Sodium starch glycollate 12.5 mg Dicalcium phosphate 167.5 mg Magnesium stearate 2.5 mg Tablet weight 250 mg.
priorityDate 2000-08-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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