FDA OKs First Generic Versions Of Cymbalta

WASHINGTON (December 11, 2013) The U.S. Food and Drug Administration said Wednesday it has approved the first generic versions of the blockbuster antidepressant drug Cymbalta, offering lower-cost access to one of the most widely prescribed treatments for depression, anxiety and other disorders.

Cymbalta is Eli Lilly & Co. Inc.'s best-selling drug.

It posted 2012 sales of $4.7 billion, making it the fifth-highest selling medication worldwide.

The drug's patent expired Thursday, clearing the way for the launch of cheaper versions of the drug from generic drug makers.

Besides depression, Cymbalta is also prescribed to treat generalized anxiety disorder, diabetic nerve pain, fibromyalgia and forms of chronic pain.

The FDA said it approved six generic versions of the pill from generic drug makers including Dr. Reddy's Laboratories Ltd., Sun Pharma Global and Teva Pharmaceuticals.


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