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NDA New Drug Application. A large document that contains all required data on the safety and efficacy of a new drug product. The NDA must be submitted to the FDA for approval before the product can be sold in the US
Ãâó: www.drscholls.com/content/info/glossary.htm
NDA following phase III of clinical testing, the drug sponsor applies for a new drug application, which is reviewed by the FDA. If the FDA finds the results favorable, the drug company can market the drug for conditions/ diseases, which are applicable to phase testing results.
Ãâó: www.therubins.com/geninfo/Definit.htm
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Ãâó: www.politicalinformation.net/encyclopedia/States_o...
NDA New Drug Application, a complete application (typically thousands of pages long) to the FDA (Food and Drug Administration) to begin marketing of a drug product in the US.
Ãâó: www.genelabs.com/resources/glossary.html
Nd No Date; no publication date is supplied in the book.
Ãâó: www.ioba.org/terms.html
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