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Atomoxetine
Venkatasai is a leading provider of pharmaceutical reference standards, specializing in the supply of high-purity Atomoxetine 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 Atomoxetine -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.
Atomoxetine Hydrochloride
Atomoxetine EP Impurity A (HCl)
Atomoxetine EP Impurity B (HCl)
Atomoxetine EP Impurity C
Atomoxetine EP Impurity D
Atomoxetine EP Impurity E
Atomoxetine EP Impurity F
Atomoxetine EP Impurity G
Atomoxetine EP Impurity H
Atomoxetine HCl Racemate
Atomoxetine N-Desmethyl Impurity
Atomoxetine-N-amide
Atomoxetine 3-Fluoro Impurity Racemate
Atomoxetine Related Compound B
Atomoxetine Related Compound C
Desmethyl Atomoxetine (HCl)
Atomoxetine
Atomoxetine Related Compound B HCl
Atomoxetine N-amide impurity
Desmethyl Atomoxetine
Atomoxetine Impurity 1
Atomoxetine Impurity 3
Atomoxetine Impurity 4
4-Hydroxy Atomoxetine
4'-Hydroxy Atomoxetine-D-glucuronide
N-Desmethyl-4-Hydroxy Atomoxetine
N-Desmethyl-4-Hydroxyatomoxetine-O glucuronide
Atomoxetine EP Impurity A
Atomoxetine EP Impurity B
Atomoxetine Impurity 5