http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-S57116009-A

Outgoing Links

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_24aca9ded2638ea793d05360dde7a4a0
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P31-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-43
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K9-08
filingDate 1981-01-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f94847b16ebca960f5260aadd0a09763
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_aafa4ffedb3ae2fd979013f0b0be8f8e
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b5a0873926327bc54495832d590418d2
publicationDate 1982-07-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-S57116009-A
titleOfInvention Composition for injection
abstract PURPOSE: To prepare a composition for injection containing specific penicillanic acid sodium salt derivative useful as an antibacterial agent, having improved rate of dissolution of the above active component without losing the stability and safety as an injection, by adding L-arginine to the active component. n CONSTITUTION: The objective injection composition contains (A) 1mol of (6-[D- (α)-( 4-hydroxy-1, 5-naphthyridine-3-carboxyamido )phenylacetamido]penicillanic acid sodium salt (PC) of formula and (B) pref. 0.1W1mol, esp. 0.25W0.5mol of L- arginine. The composition is pref. freeze-dried. Since the composition has the above effects, it can be used with remarkably improved convenience, and can be administered by intramuscular injection at a rate of as high as 500mg (titer)/3ml, thereby extending the applicable range of PC. The reduction of the pain in the intramuscular injection is also expected. n COPYRIGHT: (C)1982,JPO&Japio
priorityDate 1981-01-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

Incoming Links

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Total number of triples: 23.