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Rizatriptan
Venkatasai is a leading provider of pharmaceutical reference standards, specializing in the supply of high-purity Rizatriptan 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 Rizatriptan-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.
Rizatriptan Benzoate
Rizatriptan EP Impurity A
Rizatriptan EP Impurity B
Rizatriptan EP Impurity C
Rizatriptan EP Impurity D
Rizatriptan EP Impurity E
Rizatriptan EP Impurity F
Rizatriptan EP Impurity G
Rizatriptan EP Impurity H
Rizatriptan EP Impurity I
Rizatriptan N-Methyl Adduct
Didemethyl Rizatriptan Hydrochloride
Rizatriptan Impurity 1
Rizatriptan Impurity 2
Rizatriptan Impurity 3
Rizatriptan Impurity 4
Rizatriptan Impurity 5
Rizatriptan Impurity 6
Rizatriptan Impurity 7
Rizatriptan Impurity 8
Rizatriptan - API
N-Nitroso desmethyl Rizatriptan
N-Nitroso desmethyl Rizatriptan impurity 1
Rizatriptan Impurity 9
