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Doxylamine
Venkatasai is a leading provider of pharmaceutical reference standards, specializing in the supply of high-purity Doxylamine 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 Doxylamine-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.
Doxylamine Succinate
Doxylamine EP Impurity A (HCl)
Doxylamine EP Impurity B
Doxylamine EP Impurity C (HCl)
Doxylamine EP Impurity D
Doxylamine N’-Oxide
Doxylamine N-Oxide (HCl)
Doxylamine Di-N-Oxide
N-Desmethyldoxylamine
N-Desmethyldoxylamine succinate salt
Doxylamine Dioxide
Doxylamine N, N’-Dioxide
Doxylamine-D5
Doxylamine EP Impurity A
Doxylamine EP Impurity C
N,C-Didesmethyl Doxylamine N-Nitroso
Doxylamine ethylamine N-Oxide
N-Nitroso Doxylamine
N-Nitroso N-Desmethyl Doxylamine
Doxylamine EP Impurity A (Hydrogen Succinate)
Doxylamine
