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Re: Hawk_Driver post# 268536

Thursday, 04/23/2020 2:23:48 PM

Thursday, April 23, 2020 2:23:48 PM

Post# of 430368
I agree that demonstrating bioequivalency for MARINE should be straightforward. So the question is, will the FDA require bioequivalency for REDUCE-IT assuming a higher standard must be met? It would seem FDA would/should insist on a label restriction not for use in treating CVD if the generic drug hasn’t demonstrated R-I bioequivalency.
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