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Allopurinol
Venkatasai is a leading provider of pharmaceutical reference standards, specializing in the supply of high-purity Allopurinol 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 Allopurinol-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.
Allopurinol
Allopurinol EP Impurity A
Allopurinol EP Impurity B
Allopurinol EP Impurity C
Allopurinol EP Impurity D
Allopurinol EP Impurity E
Allopurinol EP Impurity F
Allopurinol Nitrile Impurity
Allopurinol Related Compound F
Allopurinol USP Related Compound F
Allopurinol Impurity 1
Allopurinol Impurity F (Hydrate)
