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   &lt;div style="margin-top: 12pt; font-size: 1pt"&gt;&amp;#160;
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       &lt;i&gt;&lt;font style="font-family: 'Times New Roman', Times"&gt;Kadian&lt;sup style="font-size: 85%; vertical-align: text-top"&gt;&amp;#174;&lt;/sup&gt;&lt;/font&gt;&lt;/i&gt;
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       On December&amp;#160;29, 2008, the Company completed its acquisition
       of Alpharma. In connection with the acquisition of Alpharma, the
       Company and Alpharma executed a consent order (the &amp;#8220;Consent
       Order&amp;#8221;) with the U.S.&amp;#160;Federal Trade Commission
       (&amp;#8220;FTC&amp;#8221;). The Consent Order required the Company to
       divest the assets related to Alpharma&amp;#8217;s branded oral
       long-acting opioid analgesic drug
       Kadian&lt;sup style="font-size: 85%; vertical-align: text-top"&gt;&amp;#174;&lt;/sup&gt;
       to Actavis Elizabeth, L.L.C. (&amp;#8220;Actavis LLC&amp;#8221;). In
       accordance with the Consent Order, effective upon the
       acquisition of Alpharma on December&amp;#160;29, 2008, the Company
       divested the
       Kadian&lt;sup style="font-size: 85%; vertical-align: text-top"&gt;&amp;#174;&lt;/sup&gt;
       product to Actavis LLC. Actavis LLC is entitled to sell
       Kadian&lt;sup style="font-size: 85%; vertical-align: text-top"&gt;&amp;#174;&lt;/sup&gt;
       as a branded or generic product. Prior to the divestiture,
       Actavis LLC supplied
       Kadian&lt;sup style="font-size: 85%; vertical-align: text-top"&gt;&amp;#174;&lt;/sup&gt;
       to Alpharma.
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       Actavis LLC paid a purchase price of $127,500 in cash based on
       the achievement of certain
       Kadian&lt;sup style="font-size: 85%; vertical-align: text-top"&gt;&amp;#174;&lt;/sup&gt;
       quarterly gross profit-related milestones for the period
       beginning January&amp;#160;1, 2009 and ending June&amp;#160;30, 2010.
       The purchase price payment associated with each calendar quarter
       is as follows:
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   &amp;#160;
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       &lt;b&gt;Purchase&lt;br /&gt;
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   &amp;#160;
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   &amp;#160;
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       First Quarter 2009
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   &amp;#160;
   &lt;/td&gt;
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       $
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       30,000
   &lt;/td&gt;
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   &amp;#160;
   &lt;/td&gt;
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       Second Quarter 2009
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   &amp;#160;
   &lt;/td&gt;
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       $
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       25,000
   &lt;/td&gt;
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   &amp;#160;
   &lt;/td&gt;
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       Third Quarter 2009
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   &amp;#160;
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       $
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       25,000
   &lt;/td&gt;
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   &amp;#160;
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       Fourth Quarter 2009
   &lt;/div&gt;
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   &lt;td&gt;
   &amp;#160;
   &lt;/td&gt;
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       $
   &lt;/td&gt;
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       20,000
   &lt;/td&gt;
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   &amp;#160;
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       First Quarter 2010
   &lt;/div&gt;
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   &amp;#160;
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       $
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       20,000
   &lt;/td&gt;
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   &amp;#160;
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       Second Quarter 2010
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   &amp;#160;
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       $
   &lt;/td&gt;
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       7,500
   &lt;/td&gt;
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   &amp;#160;
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       The Company recorded a receivable of $115,000 at the time of the
       divestiture, reflecting the present value of the estimated
       future purchase price payments from Actavis LLC. The Company
       recorded a gain of $12,500 in the second quarter of 2010 as a
       result of the divestiture. In accordance with the agreement,
       quarterly payments are received one quarter in arrears. During
       the second quarter and first six months of 2010, the Company
       received $20,000 and $40,000, respectively, from Actavis LLC
       related to gross profit from sales during the fourth quarter of
       2009 and the first quarter of 2010. In July 2010, the Company
       received the final payment of $7,500.
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   &lt;div style="margin-top: 12pt; font-size: 1pt"&gt;&amp;#160;
   &lt;/div&gt;
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       &lt;i&gt;&lt;font style="font-family: 'Times New Roman', Times"&gt;Skelaxin&lt;sup style="font-size: 85%; vertical-align: text-top"&gt;&amp;#174;&lt;/sup&gt;
       Authorized Generic&lt;/font&gt;&lt;/i&gt;
   &lt;/div&gt;
   &lt;div style="margin-top: 6pt; font-size: 1pt"&gt;&amp;#160;
   &lt;/div&gt;
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       In January 2008, the Company entered into an agreement with
       CorePharma, LLC (&amp;#8220;CorePharma&amp;#8221;) granting CorePharma a
       license to launch an authorized generic version of
       Skelaxin&lt;sup style="font-size: 85%; vertical-align: text-top"&gt;&amp;#174;&lt;/sup&gt;
       under certain conditions.  In accordance with this agreement,
       the Company receives a fee based on CorePharma&amp;#8217;s gross
       profit, as defined by the agreement, of the authorized generic
       product. During the second quarter of 2010, the Company
       recognized revenue of $25,624
   related to the gross profit of the CorePharma
       Skelaxin&lt;sup style="font-size: 85%; vertical-align: text-top"&gt;&amp;#174;&lt;/sup&gt;
       authorized generic which is recorded in royalties. In addition,
       the Company sells the related active pharmaceutical ingredient
       to CorePharma for their manufacture of the authorized generic.
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      <ElementReferences>Reference 1: http://www.xbrl.org/2003/role/presentationRef
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Reference 2: http://www.xbrl.org/2003/role/presentationRef
 -Publisher FASB
 -Name Emerging Issues Task Force (EITF)
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