http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-03099197-A2

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K31-7048
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K9-14
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filingDate 2002-09-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ef21ce452cbb8061ee818710af0a7a1b
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a51b23c17f42882cbe1e8f0f2a1a73c8
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publicationDate 2003-12-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber WO-03099197-A2
titleOfInvention Formulations of erythromycin derivatives with improved bioavailability
abstract The present invention describes a pharmaceutical composition for controlled release of Erythromycin derivatives, which provides better bioavailability by releasing the active agent with modified crystal characteristics immediately as well as in a controlled manner over a desired period for the treatment of various types of infections. The composition in the form of matrix tablet comprises of erythromycin derivative with modified crystal characteristics which exhibits better solubility and hence imparts improved bioavailability with negligible or no gastric side effects as compared to those immediate release compositions. More particularly, the said invention relates to pharmaceutical compositions of roxithromycin.
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priorityDate 2002-05-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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