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Aciclovir
Venkatasai is a leading provider of pharmaceutical reference standards, specializing in the supply of high-purity Aciclovir 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 Aciclovir-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.
Aciclovir EP Impurity A
Aciclovir EP Impurity B
Aciclovir EP Impurity C
Aciclovir EP Impurity F
Aciclovir EP Impurity G
Aciclovir EP Impurity I
Aciclovir EP Impurity J
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Aciclovir EP Impurity L
Aciclovir EP Impurity M
Aciclovir EP Impurity N
Aciclovir Impurity O
Aciclovir EP Impurity P
Aciclovir EP Impurity Q
Aciclovir EP Impurity R
Acyclovir L-Isoleucinate
Aciclovir Impurity 1
Aciclovir Impurity 2
Aciclovir Impurity 3
Aciclovir Impurity 4
Aciclovir Impurity 5
Aciclovir Impurity 6
Aciclovir Impurity 7
