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Raltegravir
Venkatasai is a leading provider of pharmaceutical reference standards, specializing in the supply of high-purity Raltegravir 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 Raltegravir-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.
Raltegravir
Raltegravir EP Impurity A
Raltegravir EP Impurity A Hydrobromide salt
Raltegravir EP Impurity B
Raltegravir EP Impurity D
Raltegravir EP Impurity C
Raltegravir EP Impurity E
Raltegravir EP Impurity F
Raltegravir EP Impurity G
Raltegravir Mixture of G & F
Raltegravir EP Impurity H
Dimethyl Impurity
Raltegravir Potassium
Raltegravir Diketo Amine Impurity
Raltegravir Diketo Methoxy Impurity
Raltegravir Diketo Ethoxy Impurity
Raltegravir Oxidative Impurity
Raltegravir Sodium Salt
Raltegravir β-D-Glucuronide
Raltegravir Impurity 1
Raltegravir Formyl Impurity
Raltegravir Hydrazinyl Impurity
Raltegravir Propene Impurity
Raltegravir O-Methyl Impurity
Raltegravir Methyl Ester Impurity
Raltegravir Amide Impurity
