Interested to Buy Any Domain ? << Click Here >> for more details...
in pentoperazole capsules usp why assay value is substract
from dissolution
- 1 Answers
- 4399 Views
- Ranbaxy, I also Faced
- E-Mail Answers
Answer Posted / dnyaneshwar
In case of Pentaprazole Enteric coated Tablet,As per USP ( % Released at Acid stage = Assay - Content after acid stage ).
Solution : Petaprazole molecules is very unstable in 0.1 M HCl i.e highly degraded.At the time of acid stage dissolution,the release of pentaprazole will start to degrade very fastly.Release & degradation rate take place simultaneously.Thus to determine actual released at acid dissolution after 2 hrs we can determine by above formula
| Is This Answer Correct ? | 0 Yes | 0 No |
Post New Answer View All Answers
UV and PDA detector, which have less signal to noise ratio?
which are the diffrent batches in the pharmaceuticals?
While performing TOC sst analysis Zero shift disabled & sample analysis zero shift enabled why?
identification is for unknown? qualification for known? reporting for LOQ?
What is third generation HPLC Columns?
Why we used in n-butyl acetate water content terminology while in ethyl acetate we used moisture content terminology?
We use Potassium Dichromate solution for the calibration of UV-Visible Spectrophotometer in UV region. My question is to calibrate visible region which solution could be used in photometric accuracy
As per ICH related substances stability trend limit from initial to shelf life
how to qualify the impurity?
if you get peak in blank then what require to do?
What is gelatinization?
on the basis of bcs class how to proceed the solubility?
CAN WE DETERMINE THE PEAK PURITY IN GAS CHROMATOGRAPHY ANALYSIS?
why xterra column require to use at higher ph?
Explain the relations between number of carbon atoms in alkanes and retention time ?
