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Penciclovir
Venkatasai is a leading provider of pharmaceutical reference standards, specializing in the supply of high-purity Penciclovir 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 Penciclovir-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.
Penciclovir
Penciclovir Impurity A
Penciclovir Impurity B
Penciclovir Impurity C
Penciclovir Impurity D
Penciclovir Impurity E
Penciclovir Impurity F
Diethyl Decarboxylated Compound
Methyl Ethyl Decarboxylated Compound
Esterified Compound Impurity A
Esterified Compound Impurity C
Esterified Compound Impurity D
Esterified Compound Impurity E
Esterified Compound Impurity F
Esterified Compound Impurity G
Esterified Compound Impurity H
Esterified Compound Impurity I
Esterified Compound Impurity J
N-9 Condensation Compound
Acidulated Compound
Side-chain 1
Side-chain 2
Penciclovir Diol Impurity
Penciclovir Diacetyl Impurity
