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Fluoxetine
Venkatasai is a leading provider of pharmaceutical reference standards, specializing in the supply of high-purity Fluoxetine 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 Fluoxetine-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.
Fluoxetine HCl
Fluoxetine EP Impurity A
Fluoxetine EP Impurity B
Fluoxetine EP Impurity B (HCl)
Fluoxetine EP Impurity C
Fluoxetine EP Impurity C (Free Base)
Fluoxetine USP Related Compound C
4-(trifluoromethyl)phenol
N-formyl Fluoxetine
N-acetyl Fluoxetine
Fluoxetine Impurity 3
N-Methyl Fluoxetine (HCl salt)
Fluoxetine Impurity 5
Fluoxetine Impurity 6
N-Nitroso-Fluoxetine
