FDA approves Matrix NDA for Zidovudine Tablets

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FDA approves Matrix NDA for Zidovudine Tablets

news-medical.net

Mylan Inc. today announced that its subsidiary Matrix Laboratories Limited has received final approval from the U.S. Food and Drug Administration under the President's Emergency Plan for AIDS Relief for its New Drug Application for Zidovudine Tablets, 100 mg.

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Tags: HIV, AIDS, HIV Medication, STD, Diet and Nutrition, FDA, Retrovir, News

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Most Recently Shared on March 11, 2011 at 7:22 am By:

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HIV/AIDS News: FDA approves Matrix NDA for Zidovudine Tablets: Mylan Inc. today announced that its subsidiary Ma... http://bit.ly/eG4LYX

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Mylan Inc. - Mylan's Matrix Receives FDA Approval Under PEPFAR for Zidovudine Tablets, 100 mg

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Mylan's Matrix Receives Tentative FDA Approval Under PEPFAR For Lamivudine And Zidovudine Tablets, 30 Mg/60 Mg http://mnt.to/3QhS #hivaids

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news-medical.net — “Mylan Inc. today announced that its privately held Indian subsidiary, Matrix Laboratories Limited, has received tentative approval from the U.S. Food and Drug Administration (FDA) under the President's Emergency Plan for AIDS Relief (PEPFAR) for its New Drug Application (NDA) for Efavirenz, Lamivudine and Tenofovir Disoproxil Fumarate Tablets, 600 mg/300 mg/300 mg.View full resource at news-medical.net

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