This impurity is related to Gatifloxacin Desethylene Impurity 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.
       
      
        Gatifloxacin Desethylene Impurity is used as a reference standard in analytical research. It ensures consistency of formulations.
       
      
        Chemical Name:7-(2-Aminopropylamino)-1-cyclopropyl-6-fluoro-8-methoxy-4-oxo-1,4-dihydroquinoline-3-carboxylic acidCountry of Origin: India Product Category: Impurity Reference StandardAPI NAME: Gatifloxacin Molecular Formula: C17H20FN3O4
Molecular Weight: 349.4
Storage: Store in a cool, dry place.