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Re: sci101 post# 27130

Friday, 03/17/2017 2:30:34 PM

Friday, March 17, 2017 2:30:34 PM

Post# of 30393
I am wondering how Apricus can submit the new & improved shelf life data to the FDA later this year if all the company is doing in its resubmission is responding to the listed deficiencies which are not about shelf life?

Apricus' original submission to the FDA years ago certainly was based on shelf life data of the same ilk as the data submitted to Health Canada, so how can Apricus get around that old data in the original NDA and replace it with the new & improved data?
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