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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_ec8ee9b62d27aba6255e39401980041e
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P1-06
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K9-209
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-21
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P1-06
filingDate 2017-12-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a66c9bed46c6415d7ef9818b34937648
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0d8697bf6ce2cfada240148bcf235381
publicationDate 2019-06-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber GB-2569616-A
titleOfInvention Sustained release oral pharmaceutical compositions of dicycloverine
abstract Disclosed are sustained release oral pharmaceutical compositions which comprise dicycloverine hydrochloride (dicyclomine, [bicyclohexyl]-1-carboxylic acid 2-(diethylamine)ethyl ester), an anti-spasmodic, in both a core and a film coating of the composition. The core further comprises; one or more binders (e.g. celluloses, starches), one polymer present intragranular, one polymer present extragranular and one of more inactive excipients. The film coating comprises: dicycloverine or a salt thereof, a water soluble film forming polymer and one or more inactive excipients (e.g. plasticiser, opacifier, colouring agent). Both the intragranular polymer and the extragranular polymer may be either hydrophobic or hydrophilic. Preferably, the composition is in the form of a tablet. Also claimed is a method for preparing a sustained release oral pharmaceutical composition.
priorityDate 2017-12-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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