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Adipex brand prescription drugs by a prescription-only basis, and may not sell certain other prescription drugs without a physician's prescription. The Company's primary prescription drug sales are for its products approved by the Food and Drug Administration are principally to patients who 65 years of age and older. The Company sells prescription drug sales directly to pharmacies, hospitals, physicians' offices or other commercial entities. The Company believes that its business plan for developing and implementing its product development strategy and business model implementing its strategy for selling and marketing its products is appropriate. The Company sells prescription drugs primarily to consumers, and the Company intends adipex-p purchase to sell prescription drugs physicians in an appropriate manner. The Company has also developed and introduced a variety of drugs in an effort to expand distribution for its products. In January 2013, the Company acquired all of outstanding interests in a company that, October 2011, was an indirect subsidiary of the Company's former Canadian subsidiary, Teva. The acquisition was intended to extend operations of the company that has a broad range of proprietary prescription drugs marketed in several countries for an estimated $6 million. The acquisition related principally to manufacture of generic and bioengineered products for the pharmaceutical, consumer, biotechnology and cosmetic markets. The Company recognized purchase costs and related benefits of the acquisition from its Consolidated Statements of Operations for the year ended December 31, 2012, which amounted to approximately $14 million. The Company believes that a significant portion of the business will allow it to generate higher revenues from its existing products and to be able focus on products and processes for which it has the most experience. For financial purposes, the acquisition does not qualify as a sale of assets. In December 2010, the Company entered into an agreement with Gilead Sciences, Inc. to develop, market and distribute a new generation of hepatitis C treatments based on its proprietary technologies, which would also include a new generation of antivirals, both in the U.S. and internationally. agreement had the potential to generate annual sales of up to $300 million and was expected to generate revenue through 2016. For fiscal year 2012, the agreement was amended to increase the annual revenue forecast. Company estimated the potential for revenue in 2013 the agreement to range between $150 million and $200 million, adjusted its fiscal year 2013 guidance for revenue to reflect this. Gilead provided the Company with an additional $50 million through September 2011, based on Gilead's commitment of $100 million during the first year after introduction. Company is currently in the process of evaluating Gilead's financial performance. At December 31, 2012, the Company had not yet received or calculated any royalty from the sale of hepatitis C products under the canada drugs online fax number original agreement with Gilead. At December 31, 2012, the Company expected to accrue royalties for the first year of any sales based on current expectations. In August 2011, the Company entered into a license agreement with Gilead Sciences, Inc. under which the Company would develop and introduce two new hepatitis C treatments to Gilead Science, Inc. in late 2011. Gilead provided development services to the Company during 2011 and 2012. Gilead's development programs include drugs that treat hepatitis C, including one in adipex-p 37.5mg 30 $100.00 $3.33 $90.00 late 2010. During the six-month period ending 30 June 2012, Gilead contributed $75 million to support the ongoing development of Gilead's hepatitis C medicines including the Gilead brand medicines, as well Gilead's generic hepatitis C medicines. As described above, the Company plans to invest about $150 million develop its drug candidates. As of December 31, 2012, the Company is engaged in research and development activities relating to two new drug candidates for the treatment of hepatocellular carcinoma (HCC). The Company believes that it has a reasonable basis for estimating likelihood of achieving its R&D development goals, including clinical data in the second period of development. Company also intends to use its existing cash resources and additional funding to pursue further development of these new drug candidates. In December 2012, a second-party independent consultant retained by Gilead concluded that the expected cost savings associated with the development of its first two hepatitis C drug candidates are greater than the estimated cost of developing those drugs independently. The Company believes that it will realize a significant adipex to purchase cost savings in connection with the development of its two drug candidates. During 2012, the Company received royalty fees of approximately $30 million from the sale of products its subsidiaries. These royalties are reported under the Company's "Other" category on Consolidated Statements of Operations, together with other general and administrative expenses. During 2012, the Company incurred approximately $10 million in royalties associated with the sales of product from its subsidiary that is marketed for the treatment of hemophilia B and the Company also received royalty fees associated with the sale of product from its subsidiary that is Order adipex diet pills online marketed for the treatment of hemophilia A. These expenses are reported as "Other" on the Consolidated Statements of Operations, together.

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