U.S. Food and Drug Administration Approves Humalog® 200 units/mL KwikPen®
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Eli Lilly & Co. (LLY) Announces FDA Approval of Higher-Concentration Humalog KwikPen
May 27, 2015 8:31 AM EDTThe U.S. Food and Drug Administration (FDA) has approved Humalog 200 units/mL KwikPen (insulin lispro 200 units/mL; U-200), a pre-filled pen containing a concentrated formulation of Lilly's rapid-acting insulin Humalog® (insulin lispro 100 units/mL) to improve glycemic control in people with type 1 and type 2 diabetes, Eli Lilly and Company (NYSE: LLY) announced today. Humalog U-200 KwikPen marks the first FDA approval of a concentrated mealtime insulin analog.
Humalog U-200 KwikPen holds twice as many units of insulin (600 units vs. 300 units) as the U-100... More
