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Nadolol
Venkatasai is a leading provider of pharmaceutical reference standards, specializing in the supply of high-purity Nadolol 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 Nadolol-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.
Nadolol EP Impurity A
Nadolol EP Impurity B
Nadolol EP Impurity C
Nadolol EP Impurity D
Nadolol EP Impurity E
Nadolol EP Impurity F
Nadolol EP Impurity G
5,6,7,8-tetrahydronaphthalene-1,6,7-triol
5,8-Dihydro-1-naphthol
Epichlorohydrin
Nadolol Epoxide Impurity
(S)-(+)-Epichlorohydrin
Nadolol Citrate Ester
Nadolol Impurity 1
Nadolol Impurity 2
Nadolol Impurity 3
(R)-Epichlorohydrin
