Mylan Receives U.S. Approval for HIV/AIDS Treatment
September 22, 2011
Canonsburg, Pa.-based Mylan Inc. said Tuesday it has received tentative US approval for a generic version of an HIV treatment regimen. Included in the regimen are generic versions of GlaxoSmithKline PLC's Epivir (lamivudine), Gilead Sciences Inc.'s Viread (tenofovir), and Boehringer Ingelheim's Viramune (nevirapine). Mylan said its subsidiary, Matrix Laboratories Ltd., received clearance from the Food and Drug Administration through the President's Emergency Plan for AIDS Relief. Eligible for sale outside the United States, the regimen will be offered in some developing nations.
This article was provided by U.S. Centers for Disease Control and Prevention. It is a part of the publication CDC HIV/Hepatitis/STD/TB Prevention News Update. Visit the CDC's website to find out more about their activities, publications and services.
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