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HPLC acetaminophen tablets assay

Discussions about HPLC, CE, TLC, SFC, and other "liquid phase" separation techniques.

3 posts Page 1 of 1
in compliance with USP, is realy necessary make a calibration curve to quantify the samples of acetaminophen tablets? if it is necessary, what range of concentration is more adecuate for the curve, in relaton with the preparation standard of 0,01 mg/ml mentioned in USP method.
Thank in advance.
Not directed specifically to acetominophen, but once we establish linearity in a test method validation, there's no need to continually re-establish that each time.

You don't HAVE to use the USP procedures for your material; prove and validate equivalency and document it.

There's lots of stuff in the USP that is "interesting".....
ok, but if i use USP method and cuantify tablets with the formula , for example for acetaminophen "10000c(ru/rs)" using only one preparation standard, is necessary make a validation?i guess no because usp method is a validated method....

i need avoid the validation at this time, i'm begginer in this methods, do you understand me?

anyway the linearity of my standard curve resulted satisfactory in all determinate range

thanks you very much!
3 posts Page 1 of 1

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