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    <title>The Federal Register</title>
    <link>http://thefederalregister.com/b.p/agency/Food_and_Drug_Administration/2005-11-25/</link>
    <description>Daily Publications of Meetings and Rules Changes for the Federal Government</description>
    <pubDate>Sun, Nov 23 2008 11:00:00 GMT</pubDate>
    <lastBuildDate>Sun, Nov 23 2008 11:00:00 GMT</lastBuildDate>
    <webMaster>info@thefederalregister.com</webMaster>
    <item>
  <title><![CDATA[  Implantation or Injectable Dosage Form New Animal Drugs;  Boldenone]]></title>
  <link>http://thefederalregister.com/d.p/2005-11-25-05-23295</link>
  <description><![CDATA[ The Food and Drug Administration (FDA) is amending the animal 
drug regulations to reflect approval of a supplemental new animal drug 
application (NADA) filed by Fort Dodge Animal Health. The supplemental  NADA provides for<br/> [[Page 70998]]<br/>
revised labeling for the veterinary prescription use of injectable 
boldenone solution in horses.
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  <guid>http://thefederalregister.com/d.p/2005-11-25-05-23295</guid>
  <pubDate>Fri, Nov 25 2005 11:00:00 GMT</pubDate>
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<item>
  <title><![CDATA[  New Animal Drugs; Flunixin ]]></title>
  <link>http://thefederalregister.com/d.p/2005-11-25-05-23294</link>
  <description><![CDATA[ The Food and Drug Administration (FDA) is amending the animal 
drug regulations to reflect approval of a supplemental new animal drug 
application (NADA) filed by ScheringPlough Animal Health Corp. The 
supplemental NADA provides for the veterinary prescription use of 
flunixin meglumine solution by intramuscular injection for the control 
of pyrexia associated with swine respiratory disease.
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  <guid>http://thefederalregister.com/d.p/2005-11-25-05-23294</guid>
  <pubDate>Fri, Nov 25 2005 11:00:00 GMT</pubDate>
</item>
<item>
  <title><![CDATA[  New Animal Drugs; Change of Sponsor's Name ]]></title>
  <link>http://thefederalregister.com/d.p/2005-11-25-05-23297</link>
  <description><![CDATA[ The Food and Drug Administration (FDA) is amending the animal 
drug regulations to reflect a change of sponsor's name from Phoenix 
Scientific, Inc., to IVX Animal Health, Inc. In order to improve the 
accuracy of the regulations, erroneous entries for Phoenix 
Pharmaceutical, Inc., are also being removed at this time.
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  <guid>http://thefederalregister.com/d.p/2005-11-25-05-23297</guid>
  <pubDate>Fri, Nov 25 2005 11:00:00 GMT</pubDate>
</item>
<item>
  <title><![CDATA[  New Animal Drugs; Change of Sponsor's Address ]]></title>
  <link>http://thefederalregister.com/d.p/2005-11-25-05-23296</link>
  <description><![CDATA[ The Food and Drug Administration (FDA) is amending the animal 
drug regulations to reflect a change of sponsor's address for Schering
Plough Animal Health Corp.
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  <guid>http://thefederalregister.com/d.p/2005-11-25-05-23296</guid>
  <pubDate>Fri, Nov 25 2005 11:00:00 GMT</pubDate>
</item>
<item>
  <title><![CDATA[  Food Labeling: Nutrient Content Claims, Expansion of the Nutrient  Content Claim ``Lean'']]></title>
  <link>http://thefederalregister.com/d.p/2005-11-25-05-23293</link>
  <description><![CDATA[ The Food and Drug Administration (FDA) is proposing to amend 
its food labeling regulations for the expanded use of the nutrient 
content claim ``lean'' on the labels of foods categorized as ``mixed 
dishes not measurable with a cup'' that meet certain criteria for total 
fat, saturated fat, and cholesterol content. This proposal responds to 
a nutrient content claim petition submitted by Nestl[eacute] Prepared 
Foods Co. (Nestl[eacute]) under the Federal Food, Drug, and Cosmetic 
Act (the act). This action also is being taken to provide reliable 
information that would assist consumers in maintaining healthy dietary 
practices.
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  <guid>http://thefederalregister.com/d.p/2005-11-25-05-23293</guid>
  <pubDate>Fri, Nov 25 2005 11:00:00 GMT</pubDate>
</item>
<item>
  <title><![CDATA[  Agency Information Collection Activities; Proposed Collection;  Comment Request; Focus Groups as Used by the Food and]]></title>
  <link>http://thefederalregister.com/d.p/2005-11-25-05-23248</link>
  <description><![CDATA[ The Food and Drug Administration (FDA) is announcing an 
opportunity for public comment on the proposed collection of certain 
information by the agency. Under the Paperwork Reduction Act of 1995 
(the PRA), Federal agencies are required to publish notice in the 
Federal Register concerning each proposed collection of information 
including each proposed extension of an existing collection of 
information, and to allow 60 days for public comment in response to the 
notice. This notice solicits comments on focus groups as used by FDA to 
gauge public opinion. Policymakers can use focus group results to test 
and refine their ideas so they can conduct further research, as well 
as, adopt new policies and to allocate or redirect significant 
resources to support these policies.
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  <guid>http://thefederalregister.com/d.p/2005-11-25-05-23248</guid>
  <pubDate>Fri, Nov 25 2005 11:00:00 GMT</pubDate>
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