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Repaglinide
Venkatasai is a leading provider of pharmaceutical reference standards, specializing in the supply of high-purity Repaglinide 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 Repaglinide-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.
Repaglinide
Repaglinide EP Impurity A
Repaglinide EP Impurity B
Repaglinide EP Impurity C
Repaglinide Impurity C
Repaglinide EP Impurity D
Repaglinide EP Impurity E
Repaglinide M1 Metabolite
Repaglinide Impurity 1
Repaglinide Impurity 2
Repaglinide Impurity 3
2-Desisopropyl-2-phenyl Repaglinide
Repaglinide RIsomer Ethyl Ester
3-Ethoxy-4-Methoxy Carbonyl Phenyl Acetic Acid
Repaglinide Impurity 4
Repaglinide Acyl-β-D-glucuronide
Repaglinide EP Impurity C (N-acetyl-L-glutamate salt)
Repaglinide M2 metabolite
3′-Hydroxy Repaglinide(Mixture of Diastereomers)
Repaglinide Impurity 5
