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Re: DewDiligence post# 111194

Tuesday, 12/21/2010 2:34:50 PM

Tuesday, December 21, 2010 2:34:50 PM

Post# of 257253

Actually, NVS/MNTA’s Copaxone ANDA becomes actionable in about three weeks, when the Hatch-Waxman 30-month stay expires. From that point on, the FDA can issue a final approval for the ANDA, not just a tentative approval.



Are there examples where FDA approved a generic while the patent litigation continued?

ij

There are times when rules and precedents cannot be broken; others when they cannot be adhered to with safety. (Thomas Joplin)

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