Losartan EP Impurity B

Losartan EP Impurity B product with CAS: 160514-13-6 is also known as Losartan Hydroxy Impurity; Candesartan Hydroxy Impurity. This product can be used as a working standard or secondary reference standard (additional internal validation as per respective FDA regulations/guidelines may require). Losartan EP Impurity B is used in Losartan impurity profiling as per limits and threshold values specified by respective drug legislation, FDA, and pharmacopoeial guidelines during commercial production of Losartan and its related formulations. Moreover, Losartan Hydroxy Impurity is also used in the process of Abbreviated New Drug Application (ANDA) filing to FDA and toxicity study of respective drug formulation. Please also find out other impurities of Losartan developed in our R&D.