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Dexlansoprazole
Venkatasai is a leading provider of pharmaceutical reference standards, specializing in the supply of high-purity Dexlansoprazole 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 Dexlansoprazole-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.
Dexlansoprazole
Dexlansoprazole N-oxide
Dexlansoprazole Nitro Sulphoxide
Dexlansoprazole degradation impurity
Dexlansoprazole M+647 Impurity
Dexlansoprazole Sesquihydrate
Dexlansoprazole Impurity 1
Dexlansoprazole Impurity 2
Dexlansoprazole Impurity 4
Dexlansoprazole Impurity 5
Dexlansoprazole Impurity 6
Dexlansoprazole Impurity 7
Dexlansoprazole Impurity 8
Dexlansoprazole Impurity 9
Dexlansoprazole impurity B
Dexlansoprazole impurity C
Dexlansoprazole impurity D
Dexlansoprazole impurity E
