thanks for the perfect explanation🙏🏻 I have a question, is it necessary to do the disintegration test before the dissolution test?
@shifaeqalb66612 жыл бұрын
is there active limit mention in guideline ? how much active atleast should be present in tablet for dissolution test requirement? if tablet contain 5 or 25 mg active ingredient should we perform dissolution test on it or not require?
@nn-yl6bd3 жыл бұрын
I do thank you for sharing this🌷
@aniketsingh13713 жыл бұрын
Sir, can you please tell me about the use of chlorpheniramine tablets in USP apparatus type 3? is it removed from USP as I could not find any source of access. pp
@takeshiinoue41052 жыл бұрын
Chlorpheniramine Maleate ER Tablets RS was announced to be discontinued on December 20, 2012. The 30 dips per minute test is no longer required in the Performance Verification Test for USP Instrument 3.
@takeshiinoue41052 жыл бұрын
Effective February 1, 2012, USP has removed the requirement for Apparatus 3 Performance Verification Test Apparatus Suitability section of General Chapter Dissolution. The change was necessary because the supply of current lot G1J218 has been depleted and no suitable replacement has been found.