This impurity is related to Levetiracetam EP Impurity A is provided with comprehensive characterization data in accordance with regulatory guidelines. It is suitable for use in analytical method development, method validation (AMV), Quality Control (QC) applications for Abbreviated New Drug Applications (ANDA) and commercial production of Asenapine.
Levetiracetam EP Impurity A is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name:(2RS)-2-(2-Oxopyrrolidin-1-yl)butanoic acidCountry of Origin: India Product Category: Impurity Reference StandardAPI NAME: Levetiracetam Molecular Formula: C8H13NO3
Molecular Weight: C8H13NO3
Storage: Store in a cool, dry place.