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Abstract
The objective of current study was to develop and validate stability indicating UV Spectrophotometric and RP-HPLC method for Calcipotriene in bulk drug and pharmaceutical formulation. UV Spectrophotometric method was developed utilizing Analytical Technologies limited. Detection was carried out at absorption maxima at 260nm using methanol as a solvent. Beer’s law was followed in the concentration range of 5-25 µg/mL, and the drug was quantitated using A1% 1cm at 260 nm, which produced a correlat

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