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      03-10-2014, 08:52 PM   #137
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Quote:
Originally Posted by 1MOREMOD View Post
Unless something has changed that's not correct, bioequivelance has to be established with a generic which includes rates of dissoution and such. Dosage form has to regulate absorbtion in the same way or peak times would be delayed or higher or lower as well. Especially with a sustained release formulation. Inactive ingredients can be whatever they want but that doesn't matter in the scheme of things.
I was in the process of changing my post as you responded. I was quick to respond without proofing. I did in fact mean bioequivalance however it's method of metabolism and its stabilizers are not regulated. I've been out of pharma for 12 years even though I was in Israel last year meeting with Teva
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