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Levetiracetam
Venkatasai is a leading provider of pharmaceutical reference standards, specializing in the supply of high-purity Levetiracetam 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 Levetiracetam-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.
Levetiracetam
Levetiracetam USP Related Compound A
Levetiracetam EP Impurity A
Levetiracetam EP Impurity B
Levetiracetam EP Impurity C
Levetiracetam EP Impurity D
Levetiracetam EP Impurity G
Levetiracetam S-Carboxylic Acid
Levetiracetam R-Carboxylic Acid
Levetiracetam Dehydro Acid
L-2-Aminobutyric acid
Levetiracetam Racemate
L-Threonine Amide Hydrochloride
4-Chloro-3-oxobutanoic acid
Levetiracetam Symmetric anhydride
levetiracetam Ethyl Ester
Levetiracetam EP Impurity E
Levetiracetam Impurity 2
Levetiracetam Impurity 3
Levetiracetam Impurity 4
Levetiracetam Impurity 5
Levetiracetam - Impurity G (Freebase)
Levetiracetam - Impurity E (HCl Salt)
Ethyl Carbamate
Levetiracetam Impurity 1
