http://rdf.ncbi.nlm.nih.gov/pubchem/patent/PL-171229-B1
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_024beee780595725c80afb468d9e8c21 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-52 |
| filingDate | 1993-04-28-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f8092cc51a74f469c9639ef3d7944039 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ca0c720395dd990df63bfeb22ea039cf http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_34dccf670328f77aab8e8c998490a6b9 |
| publicationDate | 1997-03-28-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | PL-171229-B1 |
| titleOfInvention | A method of producing a new pharmaceutical preparation in the form of a semi-solid PL |
| abstract | 1. The method of producing a new pharmacological preparation in a semi-solid form containing Acyclovir as the active substance, using sodium lauryl sulfate, glycerin and cetyl alcohol, characterized in that Acyclovir dissolves completely in 86% glycerins at 88 - 92 ° C by adding ß-phenylethyl alcohol, forming solution I, then an 8-10% aqueous solution of sodium lauryl sulfate is added to this solution to obtain solution II, which is then mixed with molten cetyl alcohol to form solution III, which in turn is gradually cooled with continuous mixing to 10 ° C until semi-solid form of the preparation is obtained. E N 171229 B 1 GB |
| priorityDate | 1993-04-28-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 46.