| Predicate |
Object |
| assignee |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_48848daaecd28d756d570b31aedde399 |
| classificationCPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K9-1658
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K9-1664
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P1-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K9-2068
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K9-2063
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P25-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K9-0056 |
| classificationIPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K9-16
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K9-20
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-522
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-135 |
| filingDate |
2009-09-04-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate |
2015-05-28-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f1d536eaad6a38fcc9377b092c7512a9
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6432bf77e9b8d0168c280ff3c51d4353
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7d004eb93d176e4437eb85dc7dccf45f
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_80ae69a8f501585bdbb2c16e99999f83 |
| publicationDate |
2015-05-28-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber |
ES-2536736-T3 |
| titleOfInvention |
Chewable sustained release formulations |
| abstract |
A chewable, sustained release composition comprising: (a) from 1% to 80% by weight of the active ingredient; (b) 1% to 20% by weight of zein from an aqueous zein dispersion; (c) from 1% to 70% by weight of a wax-like agent; and (d) 10% to 50% by weight of microcrystalline cellulose, pregelatinized starch, or a mixture of microcrystalline cellulose and pregelatinized starch, wherein (i) the composition is in the form of multiparticulates or tablets, (ii) the composition has a in vitro dissolution rate of the active ingredient measured by the conventional USP basket method of at most 90% of the active ingredient released after 2 hours, and (iii) the in vitro dissolution rate of the active ingredient does not require the presence of a sustained release barrier coating on tablets or multiparticulates. |
| priorityDate |
2008-09-04-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type |
http://data.epo.org/linked-data/def/patent/Publication |