Fig. 2From: Development of stability-indicating HPLC method for quantification of pharmacopeia impurities of Zuclopenthixol and characterization of its stress degradation products by LCMS/MSSpecificity chromatograms in the optimized method. Chromatogram observed while analyzing placebo solution (A) and precision level solution of zuclopenthixol spiked with impurities (0.1%)Back to article page