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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;
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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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       &lt;b&gt;Purchase&lt;br /&gt;
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   &amp;#160;
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       First Quarter 2009
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   &amp;#160;
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       $
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       30,000
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   &amp;#160;
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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
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   &amp;#160;
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       Third Quarter 2009
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   &amp;#160;
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       $
   &lt;/td&gt;
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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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   &amp;#160;
   &lt;/td&gt;
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       $
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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
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   &amp;#160;
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       Second Quarter 2010
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   &amp;#160;
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       $
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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 were received one quarter in arrears. During
       the third quarter and first nine months of 2010, the Company
       received $7,500 and $47,500, respectively, from Actavis LLC
       related to gross profit from sales during the fourth quarter of
       2009 and the first six months of 2010.
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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;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;
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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 and third quarters of 2010, the Company
       recognized revenue of $25,624 and $25,223, respectively, 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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