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FDA standards are strict and rigorous, and Onglyza all drugs, even generic ones, must meet them all before entering the market. Food and Drug Administration (FDA) warning in 2009 spurred a new crop of Reglan litigation.
The U.S. Food and Drug Administration (FDA) is supposed to ensure the safety and quality of drugs reaching the public, acting on the taxpayers' behalf. For cardiovascular death, the FDA based its decision on a postmarketing study it required when it approved empagliflozin in 2014, as an adjunct to diet and exercise to improve glycemic control in adults with type 2 diabetes. There has been a Xeloda generic approved by the FDA under the name capecitabine tablet.
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