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Sumatriptan
Venkatasai is a leading provider of pharmaceutical reference standards, specializing in the supply of high-purity Sumatriptan 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 Sumatriptan-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.
Sumatriptan
Sumatriptan Succinate
Sumatriptan EP Impurity A
Sumatriptan EP Impurity B (HCl)
Sumatriptan EP Impurity C
Sumatriptan EP Impurity D
Sumatriptan EP Impurity E
Sumatriptan EP Impurity F
Sumatriptan EP Impurity G
Sumatriptan EP Impurity H
Sumatriptan Succinate Related Compound C
Sumatriptan Carboxylic Acid Impurity
Sumatriptan 3-Hydroxy-2-Oxo Impurity
Sumatriptan Aminophenyl Impurity
Sumatriptan Hydrazine Impurity
Sumatriptan Cyanomethyl Impurity
Sumatriptan 5-Hydroxymethyl Impurity
Sumatriptan Dimethylamino Impurity
Sumatriptan EP Impurity B
Sumatriptan Dimer
Sumatriptan Impurity 1
Sumatriptan Impurity 2
Sumatriptan Impurity 3
Sumatriptan Impurity 4
Sumatriptan Impurity 5
Sumatriptan Impurity 6
Sumatriptan Impurity 7
Sumatriptan Impurity 8
Sumatriptan Impurity 9
Sumatriptan Impurity 10
Sumatriptan Impurity 11
Sumatriptan Impurity 12
Sumatriptan Impurity 13
N-Nitroso Sumatriptan EP Impurity B
