http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-10568832-B2

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_b03b63dcb77a2269515f7c17cdee4a66
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K9-2077
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K9-0056
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K9-20
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K9-00
filingDate 2017-12-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2020-02-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5b6e485ac609cf337bc87d08c47bd76e
publicationDate 2020-02-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-10568832-B2
titleOfInvention Taste-masked pharmaceutical compositions
abstract There is provided a method for preparing an orally disintegrating tablet (ODT) composition comprising microparticles of one or more taste-masked active pharmaceutical ingredient(s), rapidly-dispersing microgranules, and other optional, pharmaceutically acceptable excipients wherein the ODT disintegrates on contact with saliva in the buccal cavity in about 60 seconds forming a smooth, easy-to-swallow suspension. Furthermore, the microparticles (crystals, granules, beads or pellets containing the active) applied with a taste-masking membrane comprising a combination of water-insoluble and gastrosoluble polymers release not less than about 60% of the dose is in the stomach in about 30 minutes, thus maximizing the probability of achieving bioequivalence to the reference IR product having rapid onset of action (short T max ). A process for preparing such compositions for oral administration using conventional fluid-bed equipment and rotary tablet press is also disclosed.
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priorityDate 2004-10-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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