why would the FDa give MNTA a "heads up" about teva's application? that would be improper if the FDA is going to approve teva they would jsut approve, then mnta files for immediate injunction - that is how it works
as my previous post states - i think this is MNTA's way of getting teva's capabilities in the public domain - either they have analytics to meet criteria (and then in their opinion infringed patents) or they don't - and the public knows teva has not performed the proper tests for approval - and the lawsuit is without merit
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