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Comparative research and rigorous quality control ensure that generic versions are equivalent in purity, safety, and efficacy.
During quality control testing, Rivaroxaban impurities use analytical techniques such as HPLC methods to identify and quantify the impurities present in Rivaroxaban.
Due to different synthetic procedures, the level of Rivaroxaban impurities might vary.
Rivaroxaban impurities should be stored at a controlled room temperature between 2-8°C or as indicated on the Certificate of Analysis (CoA).
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