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Levofloxacin
Venkatasai is a leading provider of pharmaceutical reference standards, specializing in the supply of high-purity Levofloxacin 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 Levofloxacin-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.
Levofloxacin
Levofloxacin Hemihydrate
Levofloxacin Diamine Impurity
Levofloxacin EP Impurity A
Levofloxacin EP Impurity B
Levofloxacin EP Impurity C
Levofloxacin EP Impurity E
Levofloxacin EP Impurity F
Levofloxacin EP Impurity G
Levofloxacin EP Impurity H
Levofloxacin EP Impurity I
Levofloxacin EP Impurity D
Levofloxacin Impurity 1
Levofloxacin Impurity 2
Levofloxacin Impurity 3
Levofloxacin Impurity 4
Levofloxacin Impurity 5
Levofloxacin Impurity 6
Levofloxacin Related compound 7
Levofloxacin Impurity 7
Levofloxacin Impurity 8
Levofloxacin N-Oxide
Levofloxacin Impurity G
Levofloxacin Impurity 10
N-Nitroso Levofloxacin EP Impurity B
Levofloxacin Impurity 11
N-Nitroso-Levofloxacin impurity-2
Levofloxacin Hydrochloride
Levofloxacin Diamine
Levofloxacin Diformyl Impurity
