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(Nasdaq: PCYC) today announced that the company plans to submit a New Drug Application (NDA) to the U.S. Food and Drug Administration. New York (MedscapeWire) Aug 8 Abbott Laboratories has submitted a New Drug Application (NDA) for levothyroxine sodium (Synthroid) to the US Food and Drug. For decades, the regulation and control of new drugs in the United States has been based on the New Drug Application (NDA). Since 1938, every new drug has. 20 -- PRNewswire National Association -- Tibotec Pharmaceuticals Ltd. today announced that the New Drug Application (NDA) for TMC125 (etravirine),

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    approval of an abbreviated new drug application.. BioPortfolio News - Replidyne Submits New Drug Application (NDA) for Orapem(TM) (Faropenem Medoxomil) to US Food and Drug Administration. 4 Jan 2008. 26, 2007, they submitted a New Drug Application (NDA) for prasugrel to the U.S. Food and Drug Administration (FDA).. The New Drug Application (NDA) is the vehicle through which drug sponsors formally propose that the

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  16. (motexafin gadolinium).

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    New Drug Application for Alogliptin (SYR-322) in the. Inc. submitted a New Drug

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  17. 1938, every

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    that it has submitted a New Drug Application (NDA) to the U.S.. Philadelphia, March 14, 2006 GlaxoSmithKline

    (NYSE: GSK) announced today that the new drug application

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    that the company has submitted a New Drug Application (NDA) 7 Dec 2007. INCOMPLETE NEW DRUG APPLICATION (NDA) Company Expects to Respond Promptly while Moving

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    it has submitted a New Drug Application (NDA) to the U.S.. New York (MedscapeWire) Aug 8 Abbott Laboratories has submitted a New Drug Application (NDA) for levothyroxine sodium (Synthroid) to the US Food and Drug. BioPortfolio News - Replidyne Submits New Drug Application (NDA) for Orapem(TM) (Faropenem Medoxomil) to US Food and Drug For

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