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Ondansetron
Venkatasai is a leading provider of pharmaceutical reference standards, specializing in the supply of high-purity Ondansetron 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 Ondansetron-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.
Ondansetron hydrochloride dihydrate
Ondansetron EP Impurity A
Ondansetron EP Impurity A (HCl)
Ondansetron EP Impurity B
Ondansetron EP Impurity C
Ondansetron EP Impurity D
Ondansetron EP Impurity F
Ondansetron EP Impurity G
Ondansetron EP Impurity H
Ondensatron Homo Impurity
Ondensatron Impurity 1
Ondensatron Impurity 2
Ondansetron
Ondansetron EP Impurity E
Ondensatron Impurity 3
Ondensatron Impurity 4
Ondensatron Impurity 5
Ondensatron Impurity 6
Ondensatron Impurity 7
Ondensatron Impurity 8
Ondensatron Impurity 9
Ondensatron Impurity 10
7-Hydroxy Ondansetron
