Predicate |
Object |
assignee |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_44e0905262f429c7590b40df8448c0c5 |
classificationCPCAdditional |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K9-5015 |
classificationCPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K9-5089 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P29-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K9-5073 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K9-5047 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K47-14 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P25-04 |
classificationIPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K47-38 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K47-14 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K9-62 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-137 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K9-26 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K9-36 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K9-50 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K9-54 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K9-52 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-135 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K9-22 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K9-20 |
filingDate |
1999-12-23-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4aeff1785497dd89e7e3fc73813cfc9a http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f0474374d26946fdfb01332276bff706 |
publicationDate |
2000-09-20-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber |
EP-1020186-A3 |
titleOfInvention |
Sustained release tramadol preparations with a storage stable release profile and process for their manufacture |
abstract |
The invention relates to processes for the preparation of an oral, delayed-release preparation from tramadol or a physiologically tolerable salt of tramadol with a storage-stable active substance release profile by coating the active substance preparation with an aqueous ethyl cellulose dispersion which comprises at least one physiologically tolerable, lipophilic diester from an aliphatic or aromatic Contains dicarboxylic acid with C 6 -C 40 and an aliphatic alcohol with C 1 -C 8 as a plasticizer, and dries the coating at the usual temperatures during the coating, whereby a storage-stable drug release profile is obtained even without tempering, and possibly to increase the drug release profile without impairing the storage stability at temperatures> 35 ° C until the selected, increased active ingredient release profile is reached. |
priorityDate |
1999-01-18-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type |
http://data.epo.org/linked-data/def/patent/Publication |