-
Your RFQ cart is empty!
Valaciclovir
Venkatasai is a leading provider of pharmaceutical reference standards, specializing in the supply of high-purity Valaciclovir 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 Valaciclovir-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.
Valaciclovir Hydrochloride
Valaciclovir Hydrochloride Dihydrate
Acyclovir L-Leucinate
Valaciclovir EP Impurity A
Valaciclovir EP Impurity B
Valaciclovir EP Impurity C
Valaciclovir EP Impurity C (HCl)
Valaciclovir EP Impurity D
Valaciclovir EP Impurity E
Valaciclovir EP Impurity F
Valaciclovir EP Impurity G
Valaciclovir EP Impurity H (HCl)
Valaciclovir EP Impurity I
Valaciclovir EP Impurity J
Valaciclovir EP Impurity K
Valaciclovir EP Impurity L
Valaciclovir EP Impurity M
Valaciclovir EP Impurity N
Valaciclovir EP Impurity O
Valaciclovir EP Impurity P
Valaciclovir EP Impurity Q
Valaciclovir EP Impurity R
Valaciclovir EP Impurity S
Valaciclovir
Valaciclovir Ep Impurity F(Free Base)
Valaciclovir EP Impurity R (HCl Salt)
Valaciclovir EP Impurity H
Valacyclovir Valine Impurity
