http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-109078004-B
Outgoing Links
| Predicate | Object |
|---|---|
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K31-5513 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K31-407 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K9-2063 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K9-2095 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K9-0056 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K9-20 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-5513 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-407 |
| filingDate | 2017-06-13-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 2021-05-04-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 2021-05-04-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | CN-109078004-B |
| titleOfInvention | Freeze-dried orally disintegrating tablet and preparation method thereof |
| abstract | The invention relates to a freeze-dried orally disintegrating tablet and a prescription and a process for preparing the freeze-dried orally disintegrating tablet by adopting a freeze-drying method, wherein the unit dose comprises 1 mg-50 mg of active ingredients unstable to acidity or alkalinity, 1 mg-40 mg of skeleton propping agent and 1 mg-40 mg of enzymolysis gelatin. The preparation method has the advantages of simple and easy process, good taste and short disintegration time. After 21 days of lofting, the total amount of impurities of the freeze-dried orally disintegrating tablet prepared by the invention is lower than 0.34 percent under the conditions of high temperature, high humidity and illumination, all the impurities do not exceed the limit requirements of the impurities, and the growth speed of all the impurities is slower. |
| priorityDate | 2017-06-13-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 194.