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Method development and validation for estimation of rufinamide in tablet dosage forms by RP-HPLC
2016
International Journal of Pharmaceutical Chemistry and Analysis
A simple, precise, rapid and reproducible stability indicating RP -HPLC method was developed and validated for the determination of Rufinamide in pharmaceutical dosage forms. Chromatography was performed on a C18 (ODS) Acetonitrile: water: Triethylamine buffer pH4.6: Methanol (70:20:10 v/v) was used as mobile phase and flow rate was adjusted to 0.8 ml/ min. The detection was carried out at 292 nm using analytical Tech. UV-Visible detector SpD-10AVP. The obtained calibration curve was linear in
doi:10.5958/2394-2797.2016.00015.0
fatcat:77t23d7qerfcde4wocu6c3viey