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Doxorubicin
Venkatasai is a leading provider of pharmaceutical reference standards, specializing in the supply of high-purity Doxorubicin 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 Doxorubicin-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.
Doxorubicin Hydrochloride
Doxorubicin EP Impurity A
Doxorubicin EP Impurity B
Doxorubicin EP Impurity C
Doxorubicin Hydrobromide EP Impurity C
Doxorubicin EP Impurity D
Doxorubicin Mixture of Diastereomers
Doxorubicin Dimer Impurity 1
Doxorubicin Dimer Impurity 2
Doxorubicin Dimer Impurity 3
Doxorubicin Impurity-ll
9-Carboxy Doxorubicin Impurity
Doxorubicin Olefin Impurity
Doxorubicin Impurity 13
Doxorubicin Impurity 14
Doxorubicin Impurity 15
Doxorubicin Impurity 16
Doxorubicin
