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Zidovudine
Venkatasai is a leading provider of pharmaceutical reference standards, specializing in the supply of high-purity Zidovudine 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 Zidovudine-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.
Zidovudine EP Impurity A
Zidovudine EP Impurity B
Zidovudine EP Impurity C
Zidovudine EP Impurity D
Zidovudine EP Impurity E
Zidovudine EP Impurity F
Zidovudine EP Impurity G
Zidovudine EP Impurity J
Zidovudine EP Impurity K
Zidovudine Impurity 1
3’-Amino-3’-deoxythymidine
