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Desogestrel
Venkatasai is a leading provider of pharmaceutical reference standards, specializing in the supply of high-purity Desogestrel 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 Desogestrel-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.
Desogestrel
Desogestrel EP Impurity A
Desogestrel EP Impurity B
Desogestrel EP Impurity C
Desogestrel EP Impurity D
Desogestrel EP Impurity E
Etonogestrel Sulfate Sodium Salt
17-β-Desogestrel
Methyl Gestodene
Desogestrel Impurity 1
Desogestrel Impurity 2
Desogestrel Impurity 3
Desogestrel Impurity 4
Desogestrel Impurity 5
Desogestrel Impurity 6
