http://rdf.ncbi.nlm.nih.gov/pubchem/patent/AT-388101-B
Outgoing Links
Predicate | Object |
---|---|
assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_bba842fc4d37dfcaced1b55bc0c91c7c |
classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K9-4858 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K9-4866 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K31-48 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K9-48 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K47-44 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K9-52 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K47-14 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K9-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-48 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K9-22 |
filingDate | 1986-02-04-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
grantDate | 1989-05-10-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationDate | 1989-05-10-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | AT-388101-B |
titleOfInvention | METHOD FOR PRODUCING A PHARMACEUTICAL COMPOSITION FOR ORAL ADMINISTRATION WITH CONTROLLED ACTIVE SUBSTANCE RELEASE |
abstract | A process for the production of a pharmaceutical composition for oral administration with controlled release of the active ingredient, with addition of swelling agents and fatty materials is described and entails a 9,10-dihydro-ergot alkaloid active ingredient being mixed with a hydrophilic, swellable, pharmaceutically acceptable substance and with a pharmaceutically acceptable fatty material, and where appropriate with other additives and, where appropriate, being further processed to capsules or tablets. |
priorityDate | 1985-02-05-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 44.