Source:http://linkedlifedata.com/resource/pubmed/id/10316827
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Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4
|
pubmed:dateCreated |
1979-7-28
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
H
|
pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
May
|
pubmed:issn |
0020-9546
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
20
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
11, 13
|
pubmed:dateRevised |
2000-12-18
|
pubmed:meshHeading |
pubmed-meshheading:10316827-Legislation, Drug,
pubmed-meshheading:10316827-Pharmaceutical Preparations,
pubmed-meshheading:10316827-Public Policy,
pubmed-meshheading:10316827-Therapeutic Equivalency,
pubmed-meshheading:10316827-United States,
pubmed-meshheading:10316827-United States Food and Drug Administration
|
pubmed:year |
1979
|
pubmed:articleTitle |
Generic vs. brand name drugs--defining and enforcing standards.
|
pubmed:publicationType |
Journal Article
|