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Nifedipine
Venkatasai is a leading provider of pharmaceutical reference standards, specializing in the supply of high-purity Nifedipine 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 Nifedipine-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.
Nifedipine Phenylpyridine Analog
Nifedipine Monoamide
Nifedipine Pyrimidine Impurity
Nifedipine EP Impurity A
Nifedipine EP Impurity B
Nifedipine EP Impurity C
Nifedipine EP Impurity D
Nifedipine Impurity 1
Nifedipine Impurity 2
Nifedipine Impurity 3
Nifedipine Impurity 4
Nifedipine Impurity 5
Nifedipine Impurity 6
Nifedipine Nitroso Impurity
N-Nitroso piperidine Impurity
Nifedipine Impurity 7
Nifedipine EP Impurity C (Z-Isomer)
Nifedipine EP Impurity D (E Isomer)
