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The FDA, recognizing this issue, has prioritized reviewing generic applications for drugs in short supply, as seen with its recent approval of exenatide (Byetta) by Amneal Pharmaceuticals and Tevas earlier launch of an authorized generic version of Victoza in the U.S

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Judge Karen Marston is expected to move the litigation toward the next stage of coordinated discovery and begin identifying representative cases that could eventually be prepared for bellwether trial testing

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