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The study aims to develop and validate a reliable RP-HPLC method for estimating Ivermectin in cream formulation. Key objectives include optimizing chromatographic conditions and validating the analytical method per standard guidelines. The methodology involved using a Sunfire C18 column and an isocratic mobile phase, resulting in a well-resolved peak for Ivermectin with a retention time of approximately 2.8 minutes.

Author

bibd22121625

Language

EN