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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D411-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D411-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K9-20
filingDate 2009-09-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_dd29b19608acdf9abb944527f291e95d
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publicationDate 2011-05-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber BR-PI0903664-A2
titleOfInvention Method of obtaining a new crystalline form of lamivudine, its monohydrate hydrochloride salt, pharmaceutical formulations and their uses
abstract METHOD OF OBTAINING A NEW CRYSTALLINE FORM OF LAMIVUDINE, ITS MONOHYDRATED CHLORIDRAATE SALT, PHARMACEUTICAL FORMULATIONS AND ITS USES. The present invention is intended for the method of obtaining a solid crystalline form of lamivudine, form VI, its hydrochloride salt monohydrate and its pharmaceutical formulations. In addition, the present application relates to the use of the crystalline forms of lamivudine monohydrate salt in the preparation of drugs indicated as an anti-HIV agent (acquired immunodeficiency syndrome - AIDS).
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-9688666-B2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2015368232-A1
priorityDate 2009-09-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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