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Ramipril
Venkatasai is a leading provider of pharmaceutical reference standards, specializing in the supply of high-purity Ramipril 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 Ramipril-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.
Ramipril EP Impurity A
Ramipril EP Impurity B
Ramipril EP Impurity C
Ramipril EP Impurity D
Ramipril EP Impurity E
Ramipril EP Impurity F
Ramipril EP Impurity G
Ramipril EP Impurity H
Ramipril EP Impurity I
Ramipril EP Impurity J
Ramipril EP Impurity K
Ramipril EP Impurity L
Ramipril EP Impurity M
Ramipril EP Impurity N
Ramipril EP Impurity O
Ramipril Bicyclic Acid Benzyl Ester (HCl Salt)
Ramipril Bicyclic Acid
Ramipril Meglumine Amide
Ramipril Acyl Glucuronide
Ramiprilat Acyl Glucuronide
Ramipril Isomer 1
Ramipril Impurity 1
Ramipril Impurity 2
Ramipril Impurity 3
Ramipril Impurity 4
Ramipril Impurity 5
Ramipril Impurity 6
Ramipril Impurity 7
Ramipril Impurity N
Ramipril Impurity O
N-Nitroso Ramipril
Ramipril EP Impurity C (HCl)
Ramipril Benzyl Ester
