http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2009214640-A1

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_be4a9fb61ead62f4c219c5b6f202d5e0
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K9-1635
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K47-32
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filingDate 2006-03-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3878806b7016c0a85a3369105c83e5b7
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_39ac8417fedf84321cd75ad6526f1d69
publicationDate 2009-08-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-2009214640-A1
titleOfInvention Delayed release pharmaceutical oral dosage form and method of making same
abstract The present invention relates to a delayed release pharmaceutical oral dosage form and method of making same. The delayed release dosage form comprises one or more active ingredients within a granulated composition, which further comprises one or more excipients selected from the group of solid aliphatic alcohols, fatty acid esters, mixtures of esters of saturated fatty alcohols and saturated fatty acids, natural waxes, synthetic waxes, hydrogenated castor oil, hydrogenated vegetable oil, gums, and mixtures thereof; and one or more polymers or copolymers exhibiting a pH-dependent solubility. The present invention also related to method of making these delayed release dosage form.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-10258616-B2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-9993433-B2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2012059937-A1
priorityDate 2005-03-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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