ABSTRACT

The main target is to improve and authenticate a easy, sensitive, convenient, worth-while and particular method for the determination of Favipiravir and bulk and formulation using 0.1N NaOH as solvent. The method developed obeys Beer’s law at ? max of 238nm and the concentration ranges from 1-15 ?g/ml. The correlation coefficient is R2=0.9984 follows the regression equation as y=0.0544x-0.0039. According to ICH guidelines the method developed was validated for linearity, robustness, ruggedness, precision, LOD, LOQ and accuracy. As per the outcomes of the experiment, the process established is up to date, valid and diplomatic and be used for the approximation of Favipiravir in bulk and commercial dosage form. Keywords: Favipiravir, Validation, UV Spectrophotometer, Linearity, Accuracy
Publication date: 01/07/2022

https://ijbpas.com/pdf/2022/July/MS_IJBPAS_2022_6199.pdf

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https://doi.org/10.31032/IJBPAS/2022/11.7.6199