Research Article
A Validated RP-HPLC Stability Method for the Estimation of Chlorthalidone and Its Process-Related Impurities in an API and Tablet Formulation
Table 6
Results for the % recovery with the chlorthalidone tablets.
| ā | % recovery | 50% | 100% | 150% |
| Stage II process impurity | 100.03 | 98.39 | 98.71 | 99.29 | 99.34 | 99.44 | 99.49 | 100.47 | 100.71 | Mean % recovery | 99.05 | 99.36 | 100.22 | SD | 4689.33 | 815.064 | 10458.61 | %RSD | 0.8776 | 0.0760 | 0.6447 | Stage III process impurity | 98.91 | 98.89 | 98.60 | 99.45 | 99.63 | 99.91 | 98.80 | 99.22 | 99.66 | Mean % recovery | 98.25 | 99.62 | 99.23 | SD | 1035.37 | 1819.20 | 6980.63 | %RSD | 0.194 | 0.169 | 0.434 |
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