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Levosimendan
Venkatasai is a leading provider of pharmaceutical reference standards, specializing in the supply of high-purity Levosimendan 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 Levosimendan-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.
Levosimendan
Levosimendan Dimer
Levosimendan Impurity 3
Levosimendan Impurity 4
Levosimendan Impurity 5
Levosimendan Impurity 6
Levosimendan Impurity 7
Levosimendan Impurity 8
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Levosimendan Impurity 11
Levosimendan Impurity 15
Levosimendan Impurity 16
Levosimendan Impurity 12
Levosimendan Impurity 13
Levosimendan Related Compound F
