http://rdf.ncbi.nlm.nih.gov/pubchem/patent/DK-174540-B1

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_cf32b60391b469c41e86c353437f5751
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K38-23
filingDate 1990-05-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2003-05-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_fa3e850b4e981b253f25d8989de69fe6
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b0dcf28aae6c0761ada823ac895cbb13
publicationDate 2003-05-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber DK-174540-B1
titleOfInvention Process for Preparing a Liquid Pharmaceutical Preparation Containing Calcitonin and Container Containing Such Preparation
abstract Pharmaceutical compsns. for admin. intranasally, such as a liquid nasal spray, contain a calcitonin (I), a benzalkonium chloride and a suitable liquid diluent or carrier. (I) is derived from fish, esp. salmon or eels, humans, or pigs. That derived from salmon is preferred. The preferred concentration of the benzalkonium chloride is 0.003-0.03% w/v. Other materials that may be present include surfactants, preservatives, oiliary stimulants and pH regulators. The unit dose of (I) is 50-400 MRC units, given at a rate between once per day and 3 times per week. The total volume given per admin. is pref. between 0.05 and 0.15 ml. (I) is known for the treatment of Paget's disease, hypercalcaemia, and osteoporosis. Previously, (I) needed to be administered by injection, usually intramuscularly. This was painful and inconvenient since regular administration is necessary. The present compositions allow self-medication to take place.
priorityDate 1982-10-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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