http://rdf.ncbi.nlm.nih.gov/pubchem/patent/DD-212897-A5

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_3e9445e5e3626f36e932c6451a928250
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P29-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K9-0014
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K9-10
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K45-08
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K47-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-195
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P29-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K9-10
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K9-107
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K9-00
filingDate 1983-10-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a745529b6769e9d01b1635128ecc9565
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a8bf7e9cefcfe588fd05ddd11cbf5792
publicationDate 1984-08-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber DD-212897-A5
titleOfInvention PROCESS FOR PREPARING A TOPICALLY APPLICABLE PHARMACEUTICAL COMPOSITION
abstract The invention relates to a process for the preparation of a novel, topically administrable pharmaceutical composition based on an oil / water emulsion which contains as active ingredient a non-steroidal anti-inflammatory compound for the treatment of pain, inflammation and / or rheumatism. The aim of the invention is to provide a composition which ensures a good solubility of the active ingredient and which is able to transport the active ingredient through the cornea. According to the invention, the novel compositions contain as active ingredient about 0.1 to 10% by weight of a non-steroidal anti-inflammatory compound having at least one acidic group, 10 to 50% by weight of a water-soluble, volatile lower alkanol having 2 to 4 carbon atoms , 3 to 15 wt .-% of an optionally self-emulsifying lipid, 0.5 to 2 wt .-% of a Gelgeruestbildners, 1 to 20 wt .-% of a co-solvent, 40 to 80 wt .-% water, optionally 0.5 to 5% by weight of an emulsifier if the lipid phase is not self-emulsifying and, if desired, non-essential constituents.
priorityDate 1982-10-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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