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  <FDSYS>
    <CFRTITLE>21</CFRTITLE>
    <CFRTITLETEXT>Food and Drugs</CFRTITLETEXT>
    <VOL>4</VOL>
    <DATE>2009-04-01</DATE>
    <ORIGINALDATE>2009-04-01</ORIGINALDATE>
    <COVERONLY>false</COVERONLY>
    <TITLE>Restrictions on reimportation.</TITLE>
    <GRANULENUM>203.10</GRANULENUM>
    <HEADING>Section 203.10</HEADING>
    <ANCESTORS>
      <PARENT HEADING="Title 21" SEQ="4">Food and Drugs</PARENT>
      <PARENT HEADING="CHAPTER I" SEQ="3">FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED)</PARENT>
      <PARENT HEADING="SUBCHAPTER C" SEQ="2">DRUGS: GENERAL</PARENT>
      <PARENT HEADING="PART 203" SEQ="1">PRESCRIPTION DRUG MARKETING</PARENT>
      <PARENT HEADING="Subpart B" SEQ="0">Reimportation</PARENT>
    </ANCESTORS>
  </FDSYS>
  <SECTION>
    <SECTNO>§ 203.10</SECTNO>
    <SUBJECT>Restrictions on reimportation.</SUBJECT>
    <P>No prescription drug or drug composed wholly or partly of insulin that was manufactured in a State and exported from the United States may be reimported by anyone other than its manufacturer, except that FDA may grant permission to a person other than the manufacturer to reimport a prescription drug or insulin-containing drug if it determines that such reimportation is required for emergency medical care.</P>
  </SECTION>
</CFRGRANULE>
