http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CZ-20004097-A3

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_44e0905262f429c7590b40df8448c0c5
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K9-16
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-47
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K9-20
filingDate 1999-04-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_73e8bd115a70d1b93335488e77f0587d
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2d769bf13954f0668d98efb87937e40a
publicationDate 2001-02-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CZ-20004097-A3
titleOfInvention Oral dosage forms with reproducible release of the active ingredients gatifloxacin or pharmaceutically acceptable salts or hydrates thereof
abstract The present invention relates to a solid multiparticulate dosage form for use in a pharmaceutical compositionnoral administration containing or including gatifloxacinnpharmaceutically acceptable salts or hydrates and excipientsnfrom the group comprising fillers, binders, lubricants and substancesndisintegrating agents or mixtures thereof, wherein the internal phasencontains the active ingredient gatifloxacin or a pharmaceutically acceptable salt thereofnuseful salts or hydrates together with excipientsna group of fillers, binders, disintegrants, ornmixtures thereof and that it contains at least one external phase,nnecessarily consisting of at least one disintegrant andnother excipients from the group consisting of at least onena lubricant, optionally fillers and / or optionally binders, as well asnmethod of its production.
priorityDate 1999-04-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 33.