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Oxybutynin
Venkatasai is a leading provider of pharmaceutical reference standards, specializing in the supply of high-purity Oxybutynin 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 Oxybutynin-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.
Oxybutynin
Oxybutynin Hydrochloride
2-Chloro Oxybutynin
3-Chloro Oxybutynin
Oxybutynin EP Impurity A
Oxybutynin EP Impurity B
Oxybutynin EP Impurity F
Oxybutynin EP Impurity C
Oxybutynin EP Impurity D
Oxybutynin EP Impurity E (HCl)
Oxybutynin-N-Oxide
3-Quinuclidinyl Benzilate
N-substituted Ally Oxybutynin Impurity
Oxybutynin-N-Subsituted Allyl Impurity
Oxybutynin Impurity 1
Oxybutynin EP Impurity E
