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See Latest ArticlesTakeda Provides Update on the Investigational Fixed-Dose Combination of alogliptin and ACTOS (pioglitazone HCl)
Takeda Pharmaceuticals North America, 07/28/09
akeda Pharmaceutical Company Limited announced that Takeda Global Research and Development Center, Inc., a wholly owned United States subsidiary, received notification from the U.S. Food and Drug Administration that the FDA extended the review of the New Drug Application for the fixed–dose combination of alogliptin and ACTOS. The new Prescription Drug User Fee Act date for the FDC is September 2009.
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