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Rifaximin
Venkatasai is a leading provider of pharmaceutical reference standards, specializing in the supply of high-purity Rifaximin 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 Rifaximin-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.
Rifaximin
Rifaximin EP Impurity A
Rifaximin EP Impurity B
Rifaximin EP Impurity C
Rifaximin EP Impurity D
Rifaximin EP Impurity E
Rifaximin EP Impurity F
Rifaximin EP Impurity G
Rifaximin EP Impurity H
25-Desacetyl Rifampicin
25-Desacetyl-21-acetyl rifampicin
25-Desacetyl Rifaximin
Rifaximin Impurity 1
Rifaximin Impurity 2
