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Thursday, 07/06/2017 7:38:27 AM

Thursday, July 06, 2017 7:38:27 AM

Post# of 8460
TNXP as said, don't mess up w/solid companies On July 6, 2017, Tonix Pharmaceuticals Holding Corp. (the “Company”) issued a press release announcing that the Company received conditional acceptance from the U.S. Food and Drug Administration (the “FDA”) for the proposed trade name Tonmya ® for TNX-102 SL (cyclobenzaprine HCl sublingual tablets) for the management of posttraumatic stress disorder (“PTSD”). A request for proprietary name review for Tonmya will be submitted once the PTSD New Drug Application (“NDA”) is submitted. The FDA’s final approval of Tonmya is subject to NDA approval.

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