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  <titleInfo>
    <title>Generic and innovator drugs</title>
    <subTitle>a guide to FDA approval requirements</subTitle>
  </titleInfo>
  <name type="personal">
    <namePart>Beers, Donald O.</namePart>
    <role>
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    <place>
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    <publisher>Aspen Publ. Inc.</publisher>
    <dateIssued>2008</dateIssued>
    <edition>7th ed.</edition>
    <issuance>monographic</issuance>
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  <physicalDescription>
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    <extent>p. (loose-leaf) 26 cm.</extent>
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  <subject authority="lcsh">
    <topic>Drugs</topic>
    <topic>Generic substitution</topic>
    <topic>Law and legislation</topic>
    <geographic>United States</geographic>
  </subject>
  <subject authority="lcsh">
    <topic>Patent extensions</topic>
    <geographic>United States</geographic>
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  <subject authority="lcsh">
    <topic>Drugs</topic>
    <geographic>United States</geographic>
    <topic>Generic substitution</topic>
    <topic>Patents</topic>
  </subject>
  <classification authority="lcc">KF 3894 .G45 B443 2008</classification>
  <identifier type="isbn">0735576637</identifier>
  <identifier type="isbn">9780735576636</identifier>
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    <recordCreationDate encoding="marc">080727</recordCreationDate>
    <recordChangeDate encoding="iso8601">20160527201648.0</recordChangeDate>
    <recordIdentifier source="OCoLC">288006</recordIdentifier>
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