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New product offers two commonly used doses in a single tablet, giving physicians and patients convenient dosing options
LINCOLNSHIRE, Ill., July 31 /PRNewswire/ -- Takeda Pharmaceuticals North America, Inc. (TPNA) announced that the U.S. Food and Drug Administration (FDA) has approved the New Drug Application (NDA) for duetact(TM) (pioglitazone HCl and glimepiride), pronounced "Duet Act," for the treatment of type 2 diabetes.
Duetact combines ACTOS(R)(pioglitazone HCl) and glimepiride, two widely used diabetes medications with complementary actions, in a single tablet. ACTOS directly targets insulin resistance, a condition where the body does not efficiently use the insulin it produces; and glimepiride, a sulfonylurea, acts primarily by increasing…
Source: HighBeam Research, FDA Approves duetact(TM) (pioglitazone HCl and glimepiride) for the...