Teva and Corcept have been locked in US Hatch-Waxman proceeding for more than five years over the Israeli firm’s generic version of the originator’s Korlym (mifepristone) 300mg tablets, a process long enough for an initial trial to be vacated and Teva to be awarded US Food and Drug Administration approval for its generic, with the lapse of the agency’s 30-month stay on approval.
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