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Rivaroxaban
Venkatasai is a leading provider of pharmaceutical reference standards, specializing in the supply of high-purity Rivaroxaban reference materials. Our portfolio includes both pharmacopeial and non-pharmacopeial impurities, metabolites, stable isotope-labeled compounds, and nitrosamine derivatives (N-NO products). These reference standards play a crucial role in pharmaceutical R&D, aiding in formulation development, ANDA/DMF submissions, quality control, method validation, stability studies, and impurity profiling—including the identification and assessment of potentially genotoxic impurities.
Each Rivaroxaban-related product is rigorously characterized and delivered with a detailed Certificate of Analysis (COA) and comprehensive analytical data to ensure regulatory compliance. Upon request, we also offer EP/USP traceable standards. To maintain the highest quality standards, all materials are subject to periodic re-testing and continuous quality monitoring.
Rivaroxaban Impurity B
Rivaroxaban Impurity D
Rivaroxaban Impurity E
Rivaroxaban N-Methylphthalimide Impurity
Rivaroxaban Open-Ring Acid Impurity (HCl salt)
Rivaroxaban Open-Ring N-Methyl Impurity
Rivaroxaban Phthalamide Dimer
Rivaroxaban Phthalimido Descarbonyl Impurity
Rivaroxaban Methyl ester impurity
Rivaroxaban Methyl Oxalic Impurity
Rivaroxaban Racemic Mixture
Rivaroxaban Impurity 7
Rivaroxaban Impurity 8
Rivaroxaban Phthalimido Descarbonyl Impurity
Rivaroxaban Methyl Ester Impurity
Rivaroxaban Impurity 68
Rivaroxaban Impurity 69
Rivaroxaban Impurity 70
Rivaroxaban Impurity 71
Rivaroxaban Impurity 72
Rivaroxaban Nitroso Impurity 2
Rivaroxaban Impurity 73
Rivaroxaban Nitroso Impurity 1
Rivaroxaban N-Nitroso Amide Impurity
Rivaroxaban Impurity 74
Rivaroxaban Open-Ring Acid Impurity
Rivaroxaban Impurity 75
Rivaroxaban Nitroso Impurity 5
