MNTA: Dew, do you think MNTA's recent cash infusion may be an indication that they think FDA response on generic Lovenox will be further out than they thought? The management team cannot be that in the dark regarding FDA response. Or is it a case of "do it, when you can" mentality. Is there any information regarding Teva's and Amphastar's ANDA's? I can't find anything out there. I don't know how one can gauge the extent of their ability to characterize Lovenox.
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