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Lisinopril
Venkatasai is a leading provider of pharmaceutical reference standards, specializing in the supply of high-purity Lisinopril 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 Lisinopril-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.
Lisinopril Dihydrate
CPP Lisinopril Impurity
Lisinopril EP Impurity A
Lisinopril EP Impurity B
Lisinopril EP Impurity C
Lisinopril EP Impurity D
Lisinopril EP Impurity E
Lisinopril EP Impurity F
Lisinopril EP Impurity G
Lisinopril EP Impurity H
Lisinopril EP Impurity I
Lisinopril EP Impurity J
Lisinopril Dihydrate Impurity J
Lisinopril Impurity 1
Lisinopril Impurity 2
Lisinopril Impurity 3
Lisinopril Impurity 4
Lisinopril Impurity 5
N-Nitroso Lisinopril
Lisinopril Des-Proline Dimer-I
Lisinopril Des-Proline Dimer-II
Lisinopril Impurity 6
Lisinopril Impurity 7
Lisinopril Related Compound 5 Hydrochloride
