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filingDate 1989-06-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ef3a202e8dddc938002a24735139d56f
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publicationDate 1991-01-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H0311016-A
titleOfInvention Aqueous preparation of pyrido(1,2-a)pyrimidine derivative
abstract PURPOSE: To obtain an aqueous preparation which is used as eye drops free from local stimulation with high storage stability by using a specific concentration of a pyrido[1,2-a]pyrimidine derivative, a specific concentration of polyoxyethylene sorbitan fatty acid ester, polyethylene glycol or the like. n CONSTITUTION: The subject preparation contains 0.1 to 0.3W/V% of a compound of the formula (R is n-propyl, allyl; A is tetrazolyl, carboxyl; n is 0 to 2), 0.5 to 2.0W/V% of polyoxyethylene sorbitan fatty acid ester, 0.5 to 2.0W/V% of polyethylene glycol and 1.0 to 3.5W/V% of sodium hydrogen phosphate. The preparation does not form crystals even when stored at room temperature or in a cooled place for a long period of time without decomposition of the compound of the formula. n COPYRIGHT: (C)1991,JPO&Japio
priorityDate 1989-06-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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