http://rdf.ncbi.nlm.nih.gov/pubchem/patent/MX-369035-B

Outgoing Links

Predicate Object
assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_8712c4737b2f5c281cf3d9a5dec57962
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K31-573
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-56
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filingDate 2014-12-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8f9928016e57d008a650d7f4a2585a2b
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_bdb78f7bcfd6d411145365b42e3843ad
publicationDate 2019-10-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber MX-369035-B
titleOfInvention SOLID DOSAGE UNIT OF ORAL DISSOLUTION CONTAINING A COMPONENT OF ESTETROL.
abstract The present invention provides an oral solid pharmaceutical dosage unit having a weight of 50-1,000 mg and containing at least 0.1 mg of an estetrol component selected from estetrol, estetrol esters and combinations thereof. This solid dosage unit comprises: • 4-95% by weight of granules consisting of: - 3-80% by weight of an estetrol component selected from estetrol, estetrol esters and combinations thereof; - 20-97% by weight of C4-C12 sugar alcohol; - 0-45% by weight of one or more other pharmaceutically acceptable ingredients; and • 5-96% by weight of one or more pharmaceutically acceptable excipients. The solid dosage units of the present invention are particularly suitable for sublingual, buccal, or sublabial administration of the estetrol component.
priorityDate 2013-12-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

Incoming Links

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Total number of triples: 27.