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Bristol-Myers Squibb Company, Gilead Sciences, Inc. and Merck & Co., Inc. announced the submission of a Marketing Authorisation Application (MAA) for ATRIPLA(TM) (efavirenz 600 mg/emtricitabine 200 mg/ tenofovir disoproxil fumarate 300 mg) in the European Union to the European Medicines Agency (EMEA)

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