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Dextromethorphan
Venkatasai is a leading provider of pharmaceutical reference standards, specializing in the supply of high-purity Dextromethorphan 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 Dextromethorphan-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.
Dextromethorphan
Dextromethorphan Impurity A (HCl)
Dextromethorphan Impurity B (HCl)
Dextromethorphan Impurity C
Dextromethorphan Impurity D
(+)-3-Methoxy-N-Formylmorphinan
(R)-N-Formyl Octabase
Dextromethorphan N-Oxide Hydrochloride
Dextromethorphan Hydrobromide Monohydrate
Dextromethorphan-d3
Levomethorphan
Dextromethorphan EP Impurity A
Dextromethorphan EP Impurity B
Dextromethorphan Related Compound A
N-Formyl Octabase
Dextromethorphan EP Impurity D (Picrate Salt)
Dextromethorphan Impurity 1
10α-Hydroxy Dextromethorphan
N-Nitroso Dextromethorphan EP Impurity A
Dextromethorphan Impurity 2
Dextromethorphan Impurity 3
Dextromethorphan Impurity 4
Dextrorphan O-glucuronide
3-Hydroxymorphinan O-glucuronide
Dextromethorphan Hydrobromide
