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Sofosbuvir
Venkatasai is a leading provider of pharmaceutical reference standards, specializing in the supply of high-purity Sofosbuvir 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 Sofosbuvir-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.
Sofosbuvir Impurity SF2
Sofosbuvir Impurity S1
Sofosbuvir Impurity 8
Sofosbuvir Impurity 9
Sofosbuvir Impurity 78
Sofosbuvir Impurity 79
Sofosbuvir Impurity 80
Sofosbuvir Impurity 81
Sofosbuvir Impurity 82
Sofosbuvir Impurity 83
Sofosbuvir Impurity 84
Sofosbuvir Impurity 86
Sofosbuvir Impurity 85
Sofosbuvir Impurity 90
Sofosbuvir Impurity 91
Sofosbuvir Impurity 92
Sofosbuvir Impurity 87
Sofosbuvir Impurity 88
Sofosbuvir Impurity 89
Sofosbuvir Impurity 93
Sofosbuvir Impurity 94
Sofosbuvir O-Desisopropyl O-Ethyl Ester
Sofosbuvir o-desisopropyl o-methyl ester
Sofosbuvir N-Benzoyl Impurity
Sofosbuvir Impurity 99
