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Tamoxifen
Venkatasai is a leading provider of pharmaceutical reference standards, specializing in the supply of high-purity Tamoxifen 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 Tamoxifen-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.
Tamoxifen Citrate
Tamoxifen EP Impurity A (HCl salt)
Tamoxifen Impurity B
Tamoxifen EP Impurity C
Tamoxifen EP Impurity C Citrate
Tamoxifen EP Impurity D
Tamoxifen EP Impurity E
Tamoxifen EP Impurity F
Tamoxifen EP Impurity G
Tamoxifen EP Impurity H
4'-Hydroxytamoxifen
Tamoxifen N-oxide
(Z)-4-Hydroxy-N-Desmethyl Tamoxifen
4-Hydroxy-N-Desmethyl Tamoxifen
Didesmethyl Tamoxifen
Tamoxifen mixture of EZ isomers HCl
Tamoxifen PDP-1
Tamoxifen PDP-2
Tamoxifen PDP-3
Tamoxifen Dimer
Z-Chlorolefine
Tamoxifen Impurity 1
Tamoxifen Impurity 2
Tamoxifen
Tamoxifen EP Impurity A
N-Nitroso Tamoxifen EP Impurity F
