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Gemcitabine
Venkatasai is a leading provider of pharmaceutical reference standards, specializing in the supply of high-purity Gemcitabine 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 Gemcitabine-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.
Gemcitabine Hydrochloride
Gemcitabine EP Impurity A
Gemcitabine EP Impurity B
Gemcitabine EP Impurity C
Gemcitabine Monophosphate
Gemcitabine Dihydrogen Phosphate
5-O-Acetyl Gemcitabine
Gemcitabine Triphosphate Tri(triethylamine) Salt
5-O-Acetyl Gemcitabine
Gemcitabine -Beta uridine
Gemcitabine 5-Benzoate Impurity
Gemcitabine 3- benzoate impurity
Gemcitabine Specified Impurity 1
Gemcitabine Specified Impurity 2
Gemcitabine Specified Impurity 3
Gemcitabine Impurity 1
Gemcitabine Impurity 2
Gemcitabine Impurity 3
Gemcitabine Impurity 4
Gemcitabine Impurity 5
Gemcitabine Impurity 6
Gemcitabine Impurity 7
Gemcitabine Impurity 8
Gemcitabine Impurity 9
Gemcitabine Impurity 10
Gemcitabine Impurity 11
Gemcitabine Impurity 12
Gemcitabine
