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FDA Gives its Nod to Procysbi; Raptor Ascends

By Marie Powers
Staff Writer

Wednesday, May 1, 2013
The FDA put some lift under the wings of Raptor Pharmaceutical Corp., approving the orphan drug Procysbi (RP103, cysteamine bitartrate delayed-release) on its PDUFA date in the initial indication of nephropathic cystinosis (NC).

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