Eli Lilly and Company (NYSE: LLY) has withdrawn its supplemental New Drug Application (sNDA) from the U.S. Food and Drug Administration (FDA) for Cymbalta (R) (duloxetine HCl) for the management of chronic pain. Lilly plans to resubmit the ...
Original post: Lilly Withdraws Application For Additional U.S. Indication For ... - Medical News Today
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