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Amitriptyline
Venkatasai is a leading provider of pharmaceutical reference standards, specializing in the supply of high-purity Amitriptyline 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 Amitriptyline-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.
Amitriptyline Hydrochloride
Amitriptyline EP Impurity A
Amitriptyline EP Impurity B (HCl)
Amitriptyline EP Impurity C (HCl)
Amitriptyline EP Impurity D
Amitriptyline EP Impurity E (HCl)
Amitriptyline EP Impurity F
Amitriptyline EP Impurity G
Amitriptyline Impurity
Amitriptyline N-Oxide
N-desmethyl Amitriptyline
Amitriptyline N-Glucuronide
10-Hydroxy Amitriptyline Oxalate
Dibenzocyclo Heptenol
10-Hydroxy Amitriptyline
Amitriptyline D6 Hydrochloride
Amitriptyline
2-Benzoylphenylacetic acid
