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    <title>The Federal Register</title>
    <link>http://thefederalregister.com/b.p/agency/Drug_Enforcement_Administration/2007-12-04/</link>
    <description>Daily Publications of Meetings and Rules Changes for the Federal Government</description>
    <pubDate>Fri, Aug 22 2008 11:00:00 GMT</pubDate>
    <lastBuildDate>Fri, Aug 22 2008 11:00:00 GMT</lastBuildDate>
    <webMaster>info@thefederalregister.com</webMaster>
    <item>
  <title><![CDATA[  Ammar Sabbagh; Denial of Application ]]></title>
  <link>http://thefederalregister.com/d.p/2007-12-04-E7-23476</link>
  <description><![CDATA[
</p><p>    On June 12, 2006, the Deputy Assistant Administrator, Office of 
Diversion Control, Drug Enforcement Administration, issued an Order to 
Show Cause to Ammar Sabbagh (Respondent), of Sheridan, Oregon. The Show 
Cause Order proposed the denial of Respondent's pending application for 
a DEA Certificate of Registration as a distributor of the list I 
chemicals ephedrine and pseudoephedrine, on the ground that his 
``registration would be inconsistent with the public interest.'' Show  Cause Order at 1 (quoting 21 U.S.C. 823(h)).</p><p>    More specifically, the Show Cause Order alleged that on November 4,  2005, Respondent pled guilty to conspiring to distribute <br/>
pseudoephedrine, in violation of 21 U.S.C. 841(c)(2)(3), and 846. Id. 
at 2. The Show Cause Order thus alleged that Respondent's proposed 
sales of list I chemical products would be inconsistent with the public 
interest. Id. The Show Cause Order further informed Respondent of his  right to request a hearing on the allegations. Id.</p><p>    On June 19, 2006, th<script type="text/javascript">
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  <guid>http://thefederalregister.com/d.p/2007-12-04-E7-23476</guid>
  <pubDate>Tue, Dec 4 2007 11:00:00 GMT</pubDate>
</item>
<item>
  <title><![CDATA[  Manufacturer of Controlled Substances; Notice of Registration]]></title>
  <link>http://thefederalregister.com/d.p/2007-12-04-E7-23480</link>
  <description><![CDATA[
</p><p>    By Notice dated August 16, 2007, and published in the Federal 
Register on August 27, 2007 (72 FR 49018), Boehringer Ingelheim 
Chemicals, Inc., 2820 N. Normandy Drive, Petersburg, Virginia 23805, 
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 schedules I and II:<br/>
                    Drug                               Schedule Tetrahydrocannabinols (7370)...............  I<br/> Amphetamine (1100).........................  II<br/> Methylphenidate (1724).....................  II<br/> Methadone (9250)...........................  II<br/> Methadone Intermediate (9254)..............  II<br/> Dextropropoxyphene, bulk (nondosage forms)  II<br/>  (9273).</p>
<h3>Fentanyl (9801)............................  II</h3>
<p>    The company plans to manufacture the listed controlled substances 
in bulk for sale to its customers for formulation into finished  pharmaceuticals.</p><p>    No comments or objections have been received. DEA has considered 
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  <guid>http://thefederalregister.com/d.p/2007-12-04-E7-23480</guid>
  <pubDate>Tue, Dec 4 2007 11:00:00 GMT</pubDate>
</item>
<item>
  <title><![CDATA[  Manufacturer of Controlled Substances; Notice of Registration]]></title>
  <link>http://thefederalregister.com/d.p/2007-12-04-E7-23508</link>
  <description><![CDATA[
</p><p>    By Notice dated August 16, 2007, and published in the Federal 
Register on August 28, 2007, (72 FR 4931549316), Cerilliant 
Corporation, 811 Paloma Drive, Suite A, Round Rock, Texas 78664, 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 schedules I and II:<br/> [[Page 68194]]<br/>
                       Drug                               Schedule Cathinone (1235).................................  I<br/> Methcathinone (1237).............................  I<br/> NEthylamphetamine (1475)........................  I<br/> N,NDimethylamphetamine (1480)...................  I<br/> Aminorex (1585)..................................  I<br/> 4Methylaminorex (cis isomer) (1590).............  I<br/> GammaHydroxybutyric acid (2010).................  I<br/> Methaqualone (2565)..............................  I<br/> AlphaEthyltryptamine (7249).....................  I<br/> Lysergic acid diethylamide (7315)................  I<br/>
Marihuana (7360)...............<script type="text/javascript">
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  <guid>http://thefederalregister.com/d.p/2007-12-04-E7-23508</guid>
  <pubDate>Tue, Dec 4 2007 11:00:00 GMT</pubDate>
</item>
<item>
  <title><![CDATA[  Manufacturer of Controlled Substances; Notice of Registration]]></title>
  <link>http://thefederalregister.com/d.p/2007-12-04-E7-23510</link>
  <description><![CDATA[
</p><p>    By Notice dated July 31, 2007, and published in the Federal 
Register on August 9, 2007, (72 FR 4486044861), Chattem Chemicals, 
Inc., 3801 St. Elmo Avenue, Building 18, Chattanooga, Tennessee 37409, 
made application by letter 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 Lisdexamfetamine (1205)....................  II</p>
<h3>Remifentanil (9739)........................  II</h3>
<p>    The company plans to manufacture the listed controlled substances  in bulk for sale to its customers.</p><p>    No comments or objections have been received. DEA has considered 
the factors in 21 U.S.C. 823(a) and determined that the registration of 
Chattem Chemicals, Inc. to manufacture the listed basic classes of 
controlled substances is consistent with the public interest at this 
time. DEA has investigated Chattem Chemicals, Inc. to ensure that the 
company's registr<script type="text/javascript">
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  <guid>http://thefederalregister.com/d.p/2007-12-04-E7-23510</guid>
  <pubDate>Tue, Dec 4 2007 11:00:00 GMT</pubDate>
</item>
<item>
  <title><![CDATA[  Importer of Controlled Substances; Notice of Registration ]]></title>
  <link>http://thefederalregister.com/d.p/2007-12-04-E7-23512</link>
  <description><![CDATA[
</p><p>    By Notice dated September 21, 2007 and published in the Federal 
Register on September 27, 2007, (72 FR 54930), Chattem Chemicals, Inc., 
3801 St. Elmo Avenue, Building 18, Chattanooga, Tennessee 37409, made 
application by renewal to the Drug Enforcement Administration (DEA) to 
be registered as an importer of the basic classes of controlled  substances listed in schedule II:<br/> [[Page 68196]]<br/>
                    Drug                               Schedule Methamphetamine (1105).....................  II<br/> Phenylacetone (8501).......................  II<br/> Raw Opium (9600)...........................  II</p>
<h3>Poppy Straw Concentrate (9670).............  II</h3>
<p>    The company plans to import the listed controlled substances to 
manufacture bulk controlled substances for sale to its customers.
</p><p>    No comments or objections have been received. DEA has considered 
the factors in 21 U.S.C. 823(a) and 952(a) and determined that the 
registration of Chattem Chemicals, Inc. to import the basic classes of 
controlled substances i<script type="text/javascript">
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  <guid>http://thefederalregister.com/d.p/2007-12-04-E7-23512</guid>
  <pubDate>Tue, Dec 4 2007 11:00:00 GMT</pubDate>
</item>
<item>
  <title><![CDATA[  Manufacturer of Controlled Substances; Notice of Registration]]></title>
  <link>http://thefederalregister.com/d.p/2007-12-04-E7-23511</link>
  <description><![CDATA[
</p><p>    By Notice dated August 16, 2007, and published in the Federal 
Register on August 27, 2007, (72 FR 49020), Chemic Laboratories, Inc., 
480 Neponset Street, Building 7, Canton, Massachusetts 02021, made 
application by renewal to the Drug Enforcement Administration (DEA) to 
be registered as a bulk manufacturer of Cocaine (9041), a basic class  of controlled substance listed in schedule II.</p><p>    The company plans to manufacture small quantities of the above 
listed controlled substance for distribution to its customers for the  purpose of research.</p><p>    No comments or objections have been received. DEA has considered 
the factors in 21 U.S.C. 823(a) and determined that the registration of 
Chemic Laboratories, Inc. to manufacture the listed basic class of 
controlled substance is consistent with the public interest at this 
time. DEA has investigated Chemic Laboratories, Inc. to ensure that the 
company's registration is consistent with the public interest. The 
investigation has included inspection and tes<script type="text/javascript">
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  <guid>http://thefederalregister.com/d.p/2007-12-04-E7-23511</guid>
  <pubDate>Tue, Dec 4 2007 11:00:00 GMT</pubDate>
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