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Nortriptyline
Venkatasai is a leading provider of pharmaceutical reference standards, specializing in the supply of high-purity Nortriptyline 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 Nortriptyline-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.
Nortriptyline Hydrochloride
Nortriptyline EP Impurity A
Nortriptyline EP Impurity B
Nortriptyline EP Impurity D
Nortriptyline EP Impurity E
Nortriptyline EP Impurity F
Nortriptyline EP Impurity G
Nortriptyline EP Impurity H
Nortriptyline EP Impurity I
Nortriptyline EP Impurity J
Z-10 Hydroxynortriptyline
E-10 Hydroxynortriptyline
Nortriptyline Isopropyl Ester Impurity
Nortriptyline Methyl Ester Impurity
Nortriptyline Impurity B (HCl)
Nortriptyline EP Impurity E (HCl)
Nortriptyline EP Impurity F (HCl)
N-Nitroso Nortriptyline
N-Nitroso Nortriptyline-D3
N-Formyl Nortriptyline
