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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-47
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filingDate 2021-06-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b36fab1966bccba83e9d2c027b0554ac
publicationDate 2021-09-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-2021152057-A
titleOfInvention Medicine
abstract PROBLEM TO BE SOLVED: To provide a pharmaceutical product using a solid preparation in which lactone formation of pitavastatin or a salt thereof is suppressed. The following components (A) and (B): (A) Pitavastatin or a salt thereof; (B) One or more selected from the group consisting of carmellose and its salts, crospovidone and crystalline cellulose; This is a pharmaceutical product in which an orally disintegrating tablet containing 2.9% by mass or less of water is contained in an airtight package. [Selection diagram] None
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2020163059-A
priorityDate 2019-10-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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