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  <titleInfo>
    <title>United States pharmacopoeia (USP35) NF 30 (2012)</title>
  </titleInfo>
  <name type="personal">
    <namePart>General Medical Council</namePart>
    <role>
      <roleTerm authority="marcrelator" type="text">creator</roleTerm>
    </role>
  </name>
  <typeOfResource>text</typeOfResource>
  <originInfo>
    <place>
      <placeTerm type="text">United States</placeTerm>
    </place>
    <publisher>United States pharmacopoeia</publisher>
    <dateIssued>2012</dateIssued>
    <issuance>monographic</issuance>
  </originInfo>
  <physicalDescription>
    <extent>6013 p. ; 28 cm.</extent>
  </physicalDescription>
  <note>Include index.</note>
  <subject>
    <topic>European pharmacopoeia</topic>
    <topic>Drugs</topic>
    <topic>Medical instruments</topic>
    <topic>Microbiological test</topic>
    <topic>Pharmaceutical technical procedures</topic>
    <topic>Physical test</topic>
    <topic>chemical test</topic>
    <topic>RIPS</topic>
  </subject>
  <classification authority="ddc">615.1 PHA</classification>
  <identifier type="isbn"> (hb)</identifier>
  <recordInfo/>
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