limits for impurities Contribution from Tareq Taha written on 10/7/2008 at 00:34
hi
i want to ask in case of finished product which have no soecification in the pharmacopeia how to find limits like mefenamic acid , as a row material the specification for any impurity not more than 0.1 %, but as mefenamic capsule (USP)there is no method for related substances and thus there is no specification.
thank you
Answers to this contribution:
Answering this Contribution:
|
