<?xml version="1.0"?>
<?xml-stylesheet type="text/xsl" href="cfr.xsl"?>
<CFRGRANULE xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:noNamespaceSchemaLocation="CFRMergedXML.xsd">
  <FDSYS>
    <CFRTITLE>21</CFRTITLE>
    <CFRTITLETEXT>Food and Drugs</CFRTITLETEXT>
    <VOL>5</VOL>
    <DATE>2001-04-01</DATE>
    <ORIGINALDATE>2001-04-01</ORIGINALDATE>
    <COVERONLY>false</COVERONLY>
    <TITLE>Change in ownership of an application.</TITLE>
    <GRANULENUM>314.72</GRANULENUM>
    <HEADING>Section 314.72</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 D" SEQ="2">DRUGS FOR HUMAN USE</PARENT>
      <PARENT HEADING="PART 314" SEQ="1">APPLICATIONS FOR FDA APPROVAL TO MARKET A NEW DRUG</PARENT>
      <PARENT HEADING="Subpart B" SEQ="0">Applications</PARENT>
    </ANCESTORS>
  </FDSYS>
  <SECTION>
    <SECTNO>§ 314.72</SECTNO>
    <SUBJECT>Change in ownership of an application.</SUBJECT>

    <P>(a) An applicant may transfer ownership of its application. At the time of transfer the new and former owners are <PRTPAGE P="120"/>required to submit information to the Food and Drug Administration as follows:</P>
    <P>(1) The former owner shall submit a letter or other document that states that all rights to the application have been transferred to the new owner.</P>
    <P>(2) The new owner shall submit an application form signed by the new owner and a letter or other document containing the following:</P>
    <P>(i) The new owner's commitment to agreements, promises, and conditions made by the former owner and contained in the application;</P>
    <P>(ii) The date that the change in ownership is effective; and</P>
    <P>(iii) Either a statement that the new owner has a complete copy of the approved application, including supplements and records that are required to be kept under § 314.81, or a request for a copy of the application from FDA's files. FDA will provide a copy of the application to the new owner under the fee schedule in § 20.42 of FDA's public information regulations.</P>
    <P>(b) The new owner shall advise FDA about any change in the conditions in the approved application under § 314.70, except the new owner may advise FDA in the next annual report about a change in the drug product's label or labeling to change the product's brand or the name of its manufacturer, packer, or distributor.</P>
    <APPRO>(Collection of information requirements approved by the Office of Management and Budget under control number 0910-0001)</APPRO>
    <CITA>[50 FR 7493, Feb. 22, 1985; 50 FR 14212, Apr. 11, 1985, as amended at 50 FR 21238, May 23, 1985]</CITA>
  </SECTION>
</CFRGRANULE>
