http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-H03153623-A
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_2ca2e4410855da087e11bf3eea8933fa |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P31-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P1-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K47-34 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P11-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P1-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P29-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K47-44 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K9-107 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K47-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K47-02 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K45-08 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K9-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P25-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K47-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P31-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P31-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P1-10 |
| filingDate | 1989-11-09-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_be230f43e5a4b18e5bdee44be3387a8d |
| publicationDate | 1991-07-01-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | JP-H03153623-A |
| titleOfInvention | New drug transport system |
| abstract | PURPOSE: To obtain a semisolid pharmaceutical composition for oral administration, comprising a drug, a liquid which is not water and a paste capable of forming a semisolid having a hardness of a pudding together with the liquid, readily administrable in a high dose and masking an unpleasant taste. n CONSTITUTION: This composition comprises (A) a drug selected from among an antacid, an antiobese agent, antimicrobial agent, an analgesic agent, an antihistaminic agent and a decongestant, a antitussive agent, an antiinflammatory agent, an antiviral agent, an antifungal agent, a stegnotic agent, a laxative and antiasthmatic agent in an orally effective amount, usually about 0.01 to about 35wt.%, preferably about 0.1 to about 10wt.%, (B) a physiologically permissible liquid which is not water, preferably an edible oil in an amount of usually about 45 to about 99wt.%, preferably about 75 to about 90wt.% and (C) a paste capable of forming a semisolid having a hardness of a pudding together with the component B, e.g. a colloidal silicon dioxide, aluminum stearate or a high-molecular weight polyethylene glycol in an amount of usually about 1 to about 20wt.%, preferably about 3 to about 6wt.%. The composition is useful for orally administering the drug to an infant, a child or a hyposthenic patient. n COPYRIGHT: (C)1991,JPO |
| priorityDate | 1989-11-09-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 34.