http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CZ-20041002-A3
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_34fadf00cbf436daf378c00070f76020 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P5-20 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K9-2009 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P5-32 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K31-138 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K9-2054 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-138 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K9-16 |
| filingDate | 2004-09-30-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6825ebf51ae08182550f09e415fc72cc http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d78eaefa20b80bc74893a943c21a9a7f http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_880d480fbb9156afc0afa4bb1aaeac92 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9636ece3d551e1aafcc632d644eb6629 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_da46c51bbb947e8f311e94a3a1c1344c http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_930650703e1ebc2003eb84f1c1d8027d |
| publicationDate | 2006-05-17-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | CZ-20041002-A3 |
| titleOfInvention | A method for preparing an oral solid dosage form and an oral solid dosage form prepared by this method |
| abstract | A process for the preparation of an oral solid dosage form capable of immediate release of an active substance which is a water-soluble antiestrogen, in particular tamoxifen citrate, is admixed with a water-insoluble and / or alcohol-insoluble filler and optionally with at least one other pharmaceutically acceptable excipient. the filler or mixture thereof with at least one other pharmaceutically acceptable excipient has a size of less than 355 microns and no more than 10% of these particles have a size of less than 40 microns, then the triturate obtained is mixed with a water-soluble and / or alcohol-soluble filler and water-soluble or and the mixture obtained is granulated in the presence of water and / or alcohol which are used in an amount not greater than 8% by weight and the granulate obtained is dried. The oral solid dosage forms thus prepared are described. |
| priorityDate | 2004-09-30-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 53.