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Vigabatrin
Venkatasai is a leading provider of pharmaceutical reference standards, specializing in the supply of high-purity Vigabatrin 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 Vigabatrin-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.
Vigabatrin Formyl impurity
Povidone EP Impurity A
Vigabatrin Hydrochloride
Vigabatrin Hydrobromide
Vigabatrin Sulfate
Vigabatrin Calcium
Vigabatrin Sodium
Vigabatrin Potassium
Vigabatrin EP Impurity A
Vigabatrin EP Impurity B
Vigabatrin EP Impurity B (HCl)
Vigabatrin Impurity C
Vigabatrin EP Impurity D
Vigabatrin EP Impurity D Hydrochloride
Vigabatrin EP Impurity D Hydrobromide
Vigabatrin EP Impurity D Sodium
Vigabatrin EP Impurity D Potassium
Vigabatrin EP Impurity D Calcium
Vigabatrin EP Impurity E
Vigabatrin Impurity F
Vigabatrin Impurity F Potassium
Vigabatrin Impurity 1
N-3-oxocarboxypentyl vinylpyrrolidinone
Vigabatrin Impurity 3
Vigabatrin Impurity 4
N-Carboxylmethyl vinylpyrrolidinone
