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Ranbaxy Gets U.S. FDA Approval for Generic AIDS Drug

May 31, 2005

Ranbaxy Laboratories today became the first Indian drug company to gain regulatory approval for a generic AIDS drug to be included in the $15 billion President's Emergency Plan for AIDS Relief (PEPFAR). The U.S. Food and Drug Administration (FDA) has granted Ranbaxy tentative approval to make and market lamivudine tablets as part of the program. Ranbaxy is seeking FDA approval of four antiretrovirals so they can be included in the program. In November, Ranbaxy pulled all its AIDS drugs from the World Health Organization's list of approved drugs after finding discrepancies in tests that had been undertaken to show that the generics were the equivalents of the brand name drugs. The company has since submitted 11 antiretrovirals for WHO approval.

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Excerpted from:
Reuters
05.31.05


This article was provided by U.S. Centers for Disease Control and Prevention
, and is a part of the publication CDC HIV/Hepatitis/STD/TB Prevention News Update.