The aim of present work was focused on development of an analytical method for estimation of drug in tablet dosage form by using RP-HPLC method. Chromatographic technique is most widely used technique for analysis of single component or multi-component formulations. The proposed methods were applied for the determination of drugs in bulk and tablet dosage form. The technique also allow for the separation as well as analysis of different drug that are present in different formulations. The technique is allowed for separation of respective drugs from the excipients contained in the formulations and thus each drug in the multi-component can be easily separated. An analytical method was developed in order to carry out the assay of drugs present in tablet formulations. Validation studies were performing in order to access the validation parameters for the analytical method developed in accordance to ICH guidelines.
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