gsk has the rld anda as of 07/2014 was the novalere anda written with rld info when submitted in 11/2014? likely not they probably got 3 or 4 rtr
Don't randomly assume such potentially farreaching things if you can't substantiate them in any way.
The ANDA has been professionally submitted by Hi-Tech and received by the FDA. To date there has been no refusal, neither temporary nor permanent. All this is publicly documented in SEC filings and other investor communications. 101 level DD.