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    <title>The Federal Register</title>
    <link>http://thefederalregister.com/b.p/agency/Drug_Enforcement_Administration/2008-06-20/</link>
    <description>Daily Publications of Meetings and Rules Changes for the Federal Government</description>
    <pubDate>Tue, Dec 2 2008 11:00:00 GMT</pubDate>
    <lastBuildDate>Tue, Dec 2 2008 11:00:00 GMT</lastBuildDate>
    <webMaster>info@thefederalregister.com</webMaster>
    <item>
  <title><![CDATA[  Importer of Controlled Substances; Notice of Registration ]]></title>
  <link>http://thefederalregister.com/d.p/2008-06-20-E8-13912</link>
  <description><![CDATA[
</p><p>    By Notice dated April 17, 2006 and published in the Federal 
Register on April 21, 2006, (71 FR 20729), and as corrected by Notice 
dated May 15, 2006, and published in the Federal Register on May 22, 
2006, (71 FR 29354), Rhodes Technologies, 498 Washington Street, 
Coventry, Rhode Island 02816, made application to the Drug Enforcement 
Administration (DEA) to be registered as an importer of the basic  classes of controlled substances in schedule II:<br/>
                    Drug                               Schedule Raw Opium (9600)...........................  II</p>
<h3>Concentrate of Poppy Straw (9670)..........  II</h3>
<p>    The company plans to import the basic classes of controlled 
substances to manufacture bulk active pharmaceutical ingredients. The 
company is registered with DEA as a manufacturer of several controlled 
substances that are manufactured from raw opium and concentrate of  poppy straw.</p><p>    Comments, objections, and requests for a hearing were received. 
However, after a thorough review of this matt<script type="text/javascript">
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  <guid>http://thefederalregister.com/d.p/2008-06-20-E8-13912</guid>
  <pubDate>Fri, Jun 20 2008 11:00:00 GMT</pubDate>
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<item>
  <title><![CDATA[  Manufacturer of Controlled Substances; Notice of Registration]]></title>
  <link>http://thefederalregister.com/d.p/2008-06-20-E8-13911</link>
  <description><![CDATA[
</p><p>    By Notice dated February 20, 2008 and published in the Federal 
Register on February 29, 2008, (73 FR 11149), Stepan Company, Natural 
Products Dept., 100 W. Hunter Avenue, Maywood, New Jersey 07607, made 
application by renewal to the Drug Enforcement Administration (DEA) to 
be registered as a bulk manufacturer of the basic classes of controlled  substances listed in schedule II:<br/>
                    Drug                               Schedule Cocaine (9041).............................  II</p>
<h3>Benzoylecgonine (9180).....................  II</h3>
<p>    The company plans to manufacture the listed controlled substances  in bulk for distribution to its customers.</p><p>    Coca Leaves (9040) has been removed as a bulk manufacturing drug  code for the company.</p><p>    No comments or objections have been received. DEA has considered  the<br/> [[Page 35153]]<br/>
factors in 21 U.S.C. 823(a) and determined that the registration of 
Stepan Company to manufacture the listed basic classes of controlled 
substances is consistent with the public<script type="text/javascript">
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  <guid>http://thefederalregister.com/d.p/2008-06-20-E8-13911</guid>
  <pubDate>Fri, Jun 20 2008 11:00:00 GMT</pubDate>
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