Author(s): Wajid Ahmad, Rihan Jawed

Email(s): Email ID Not Available

DOI: 10.52711/0975-4377.2022.00017   

Address: Wajid Ahmad*, Rihan Jawed
Department of Pharmaceutics, Institute of Pharmacy, Angola, Turkey.
*Corresponding Author

Published In:   Volume - 14,      Issue - 2,     Year - 2022


ABSTRACT:
A rapid, sensitive and accurate method for Estimation of Anti- Histamine in Tablet Dosage Form by RP-HPLC. Mobile phase was Methanol: 0.1% Ortho phosphoric acid (80:20% v/v). Flow rate was 0.9ml/min. The detection Wavelength was 227nm. The injection volume was 20-µl. The proposed method was validated for selectivity, precision, linearity, and accuracy. All validation parameters were within the acceptable range. Linearity studies for Levamisole was performed (10-60µg/ml). The %RSD for accuracy found to be less than2%. Assay was found to be 99.17 to 101.65 respectively The range of 10-60µg /ml was selected for the linearity of a standard Levamisole. The 80%, 100% and 120% levels of recovery study were selected to perform the recovery study. Linearity studies for Levamisole was performed on (10-60µg/ml).


Cite this article:
Wajid Ahmad, Rihan Jawed. Development and Validation of Stability Indicating RP-HPLC Method for Estimation of Levamisole HCl in Bulk and Tablet Dosage Form. Research Journal of Pharmaceutical Dosage Forms and Technology.2022; 14(2):111-6. doi: 10.52711/0975-4377.2022.00017

Cite(Electronic):
Wajid Ahmad, Rihan Jawed. Development and Validation of Stability Indicating RP-HPLC Method for Estimation of Levamisole HCl in Bulk and Tablet Dosage Form. Research Journal of Pharmaceutical Dosage Forms and Technology.2022; 14(2):111-6. doi: 10.52711/0975-4377.2022.00017   Available on: https://rjpdft.com/AbstractView.aspx?PID=2022-14-2-2


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DOI: 10.5958/0975-4377 


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