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    <title>The Federal Register</title>
    <link>http://thefederalregister.com/b.p/agency/Food_and_Drug_Administration/2006-12-04/</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[  New Animal Drugs For Use in Animal Feeds; Florfenicol ]]></title>
  <link>http://thefederalregister.com/d.p/2006-12-04-E6-20398</link>
  <description><![CDATA[  The Food and Drug Administration (FDA) is amending the animal 
drug regulations to reflect approval of a new animal drug application 
(NADA) filed by ScheringPlough Animal Health Corp. The NADA provides 
for the use of a florfenicol Type A medicated article by veterinary 
feed directive to formulate swine feed used for the control of 
respiratory disease.
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  <guid>http://thefederalregister.com/d.p/2006-12-04-E6-20398</guid>
  <pubDate>Mon, Dec 4 2006 11:00:00 GMT</pubDate>
</item>
<item>
  <title><![CDATA[  Oral Dosage Form New Animal Drugs; Sulfamethazine Soluble Powder]]></title>
  <link>http://thefederalregister.com/d.p/2006-12-04-E6-20404</link>
  <description><![CDATA[ The Food and Drug Administration (FDA) is amending the animal 
drug regulations to reflect approval of an abbreviated new animal drug 
application (ANADA) filed by Cross Vetpharm Group Ltd. The ANADA 
provides for use of sulfamethazine soluble powder to create a solution 
administered as a drench to swine or cattle, or in the drinking water 
of chickens, turkeys, swine, or cattle for the treatment of coccidiosis 
or various bacterial diseases.
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  <guid>http://thefederalregister.com/d.p/2006-12-04-E6-20404</guid>
  <pubDate>Mon, Dec 4 2006 11:00:00 GMT</pubDate>
</item>
<item>
  <title><![CDATA[  Agency Information Collection Activities; Proposed Collection;  Comment Request; Substances Prohibited from Use in]]></title>
  <link>http://thefederalregister.com/d.p/2006-12-04-E6-20476</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 extending OMB approval on the 
existing recordkeeping requirements for this information collection, 
regarding animal proteins prohibited in ruminant feed.
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  <guid>http://thefederalregister.com/d.p/2006-12-04-E6-20476</guid>
  <pubDate>Mon, Dec 4 2006 11:00:00 GMT</pubDate>
</item>
<item>
  <title><![CDATA[  Agency Information Collection Activities; Proposed Collection;  Comment Request; Human Tissue Intended for]]></title>
  <link>http://thefederalregister.com/d.p/2006-12-04-E6-20477</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 the information collection 
requirements relating to FDA regulations for human tissue intended for 
transplantation.
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  <guid>http://thefederalregister.com/d.p/2006-12-04-E6-20477</guid>
  <pubDate>Mon, Dec 4 2006 11:00:00 GMT</pubDate>
</item>
<item>
  <title><![CDATA[  Agency Information Collection Activities; Submission for Office  of Management and Budget Review; Comment Request;]]></title>
  <link>http://thefederalregister.com/d.p/2006-12-04-E6-20478</link>
  <description><![CDATA[ The Food and Drug Administration (FDA) is announcing that a 
proposed collection of information has been submitted to the Office of 
Management and Budget (OMB) for review and clearance under the 
Paperwork Reduction Act of 1995.
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  <guid>http://thefederalregister.com/d.p/2006-12-04-E6-20478</guid>
  <pubDate>Mon, Dec 4 2006 11:00:00 GMT</pubDate>
</item>
<item>
  <title><![CDATA[  Notice of Approval of Original Abbreviated New Animal Drug  Application; Pyrantel Pamoate Suspension]]></title>
  <link>http://thefederalregister.com/d.p/2006-12-04-E6-20399</link>
  <description><![CDATA[ The Food and Drug Administration (FDA) is providing notice 
that it has approved an original abbreviated new animal drug [[Page 70413]]<br/>
application (ANADA) filed by First Priority, Inc. The ANADA provides 
for oral use of pyrantel pamoate suspension in horses and ponies as an 
overthecounter (OTC) animal drug product for the removal and control 
of various internal parasites.
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  <guid>http://thefederalregister.com/d.p/2006-12-04-E6-20399</guid>
  <pubDate>Mon, Dec 4 2006 11:00:00 GMT</pubDate>
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