http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-1965775-A2

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_16440effcfde156994a955659e8ebbf1
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K9-2081
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P9-12
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K9-5078
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K9-50
filingDate 2006-12-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7374a574142cc3ba51a98e6631c08ef6
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_52342f3ffabde131cedcca55130b0578
publicationDate 2008-09-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-1965775-A2
titleOfInvention Oral preparation with controlled release
abstract The invention relates to a pharmaceutical pellet which comprises a spherical core containing an active ingredient with a smooth surface and a coating on the core which controls the release of the active ingredient in a pH-independent manner. With such a pellet the release of the active ingredient can follow a profile with a lag phase of 60 minutes to 840 minutes, a proportion of 5 wt. % or less of the active ingredient being released during the lag phase. The active ingredient can furthermore be released from the pellet with a profile such that after the lag phase the release of the active ingredient amounts to between 3 and 25 wt. % per hour. The active ingredient can also be in the form of a metoprolol salt.
priorityDate 2005-12-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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