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Ziprasidone
Venkatasai is a leading provider of pharmaceutical reference standards, specializing in the supply of high-purity Ziprasidone 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 Ziprasidone -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.
Ziprasidone Hydrochloride Monohydrate
Ziprasidone EP Impurity A
Ziprasidone EP Impurity B
Ziprasidone EP Impurity C
Ziprasidone EP Impurity D
Ziprasidone EP Impurity E
Ziprasidone Impurity F
Ziprasidone EP Impurity P
Ziprasidone Sulfoxide
Ziprasidone Deschloro Impurity
Ziprasidone N-Oxide
Hydroxy Ziprasidone
N-Methyl Ziprasidone
6-Chlorooxindole
Ziprasidone Keto Impurity
Ziprasidone Impurity 1
Ziprasidone Impurity 2
Ziprasidone Impurity 3
Ziprasidone Impurity 4
Ziprasidone Impurity 5
Ziprasidone Impurity 6
Ziprasidone Impurity 7
Ziprasidone Impurity 8
Ziprasidone Impurity 9
Ziprasidone Impurity 10
Ziprasidone Impurity 11
Ziprasidone Impurity 12
Ziprasidone Impurity 13
Ziprasidone Related Compound A
Ziprasidone Hydrochloride Impurity C (Sodium Salt)
Ziprasidone Related Compound F
Ziprasidone Impurity 17
Ziprasidone
