MNTA should just offer to pay the FDA the standard NDA fee - grease the wheels a bit! Seems a tad unfair that FoBs can end up in regulatory limbo for a near indefinite period of time.
Generic Lovenox is not an FoB. Perhaps you meant to say that the Lovenox application is an ANDA, which does not have a formal review timeline.
If there were a way to expedite an ANDA review by paying a fee, I’m sure NVS (the official applicant in this case) would have done that.
“The efficient-market hypothesis may be the foremost piece of B.S. ever promulgated in any area of human knowledge!”