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Ivermectin
Venkatasai is a leading provider of pharmaceutical reference standards, specializing in the supply of high-purity Ivermectin 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 Ivermectin-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.
Ivermectin
Ivermectin EP Impurity A
Ivermectin EP Impurity B
Ivermectin EP Impurity C
Ivermectin EP Impurity D
Ivermectin EP Impurity E
Ivermectin EP Impurity F
Ivermectin EP Impurity G
Ivermectin EP Impurity H
Ivermectin EP Impurity I
Ivermectin EP Impurity J
Ivermectin EP Impurity K
Ivermectin 2-epimer
24-Ethyl Ivermectin
8a-hydroperoxide Ivermectin
Ivermectin B1b
8a-Oxo Avermectin B1a
3”-O-Demethyl Ivermectin
8a-Hydroxy Ivermactin B1a
Ivermectin Impurity 1
