A RP-HPLC Method for the Analysis of Neostigmine Methylsulfate and Process-Related Impurities, Forced Degradation Studies, in the Injection Formulation

<div>Chromatogram of alkali hydrolysis of neostigmine methylsulfate API (5 mL of 0.1 N NaOH at 60°C and for 30 min).</div>

International Journal of Analytical Chemistry

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Figure 8

Figure 8: A RP-HPLC Method for the Analysis of Neostigmine Methylsulfate and Process-Related Impurities, Forced Degradation Studies, in the Injection Formulation 

Figure 8 | A RP-HPLC Method for the Analysis of Neostigmine Methylsulfate and Process-Related Impurities, Forced Degradation Studies, in the Injection Formulation 