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Mebeverine
Venkatasai is a leading provider of pharmaceutical reference standards, specializing in the supply of high-purity Mebeverine 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 Mebeverine-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.
Mebeverine HCl
Mebeverine EP Impurity A
Mebeverine EP Impurity B
Mebeverine EP Impurity C
Mebeverine EP Impurity D
Mebeverine EP Impurity E
Mebeverine EP Impurity F
Mebeverine EP Impurity G
Mebeverine EP Impurity H
Mebeverine EP Impurity I
Mebeverine EP Impurity J
Mebeverine EP Impurity K
Mebeverine EP Impurity N
Mebeverine EP Impurity O
Dimethyl Mebeverine Acid
O-Desmethyl Mebeverine Alcohol
Mebeverine
Mebeverine Impurity 1
