I think there’s a 72% probability that the FDA approves MNTA’s Copaxone ANDA before Teva’s patents expire in May 2014. (I don’t have a prediction for the next three months, as you requested.)
Regarding MYL’s ANDA, I have no insights other than to note that MYL acquired the product from India’s Natco, where approval standards for FoB’s are relatively low.
“The efficient-market hypothesis may be the foremost piece of B.S. ever promulgated in any area of human knowledge!”