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filingDate 2016-09-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ad16b6e708ddc7457502b5f73d3b1e11
publicationDate 2018-06-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber PE-20180931-A1
titleOfInvention METHOD OF CRYSTALIZATION AND BIODAVAILABILITY
abstract IT REFERS TO A COMPOSITION THAT INCLUDES i) AT LEAST ONE ACTIVE PHARMACEUTICAL INGREDIENT (API) SUCH AS ZOLEDRONIC ACID, AND ii) A MOLECULAR COMPLEX CONFORMER THAT INCREASES THE ORAL BIODAVAILABILITY OF THE API, WHERE THE TWO FORM IS A MIXTURE OF THE TWO. MOLECULAR COMPLEX CONSISTING OF ZOLEDRONIC ACID, DL-LYSINE AND WATER. SUCH COMPOSITION IS IN ORAL DOSAGE FORM AS TABLETS OR CAPSULES THAT HAVE ENTERIC COATING
priorityDate 2015-09-18-04:00^^<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: 29.