http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-6369041-B2

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K45-06
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K31-505
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K31-714
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K31-688
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P43-00
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K45-06
filingDate 2000-03-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2002-04-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5912dc8b0e42787468013cb8a9c01543
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f24df51c9f4d9962cc9520aba1a89846
publicationDate 2002-04-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-6369041-B2
titleOfInvention Oral combinations of hydroxocobalamin and folic acid
abstract A variety of conditions is known wherein vitamin B 12 is deficient, or wherein the administration of vitamin B 12 is beneficial. n Classically, once detected and if appropriate, these have been treated by the parenteral administration of vitamin B 12 as oral administration is believed to be ineffective. Available oral preparations of vitamin B 12 all contain cyanocobalamin which is less desirable than hydroxocobalamin. n In accordance with the invention, effective oral formulations are provided which include, in addition to the hydroxocobalamin, folic acid or other folate precursor. The formulation for oral administration should be such as to provide, for a given daily dose, 0.5 to 59 mg hydroxocobalamin and 0.5 to 50 mg folic acid.
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priorityDate 1999-03-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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