Why dissolution test apparatus calibration with salycilic acid tablets was stopped by FDA&USP from the year of 2009?
Answer / b.gangatharan
Salicylic acid tablets are unstable and stuck together.moreover this tablet violates the quality of analytical standards due to this property.due to this, prednisone tablet has been included instead of salicylic acid from the year of 2009 by USP&FDA.
Thanks,
B.Gangatharan
Caplin point , pondicherry.
Is This Answer Correct ? | 6 Yes | 0 No |
in stress study if your api not soluble in hcl naoh h2o2 then what require to do?
what is the method of UV cabinet CALIBRTION
How much sample concentration should i inject against diluted standard in related substances for drug product in hplc analysis
Explain about empower software of analysing?
if v use HELIUM & ARGON instead of NITROGEN as a mobile phase what happen in GC SYSTEM ?
how to develop the icp ms method? Application of icp ms?
if content uniformity passing but dissolution varrying then what is next step?
In case of dissolution test, if there is variation within 6 individual units however the batch is complying as per S1 criteria, is it necessary to do investigation for the same? What should be the criteria for such variation?
what is lod and loq ?,why use k2cr2o7 , kcl h2so4 in uv calibration ?,why use benzophenone & caffene acetone in hplc calibration ?,what is leading peak in hplc ?why we do the calibration of limit of stry light in hplc & uv ?
How to fix the sample conc. in Related substances test by HPLC?
what is mean by 21 CFR PART? In that what is 21 ?
What is linearity in HPLC and how will you test?