Development and validation of a dissolution method using HPLC for diclofenac potassium in oral suspension
The present study describes the development and validation of an in vitro dissolution method for evaluation to release diclofenac potassium in oral suspension. The dissolution test was developed and validated according to international guidelines. Parameters like linearity, specificity, precision an...
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Format: | Book |
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Universidade de São Paulo,
2014-04-01T00:00:00Z.
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A1234.567 |
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