Found 9617 Results / Page 105 of 481

Development and validation of a stability-indicating lc method for the determination of tenofovir disoproxil fumarate in pharmaceutical formulation

2012 / Songklanakarin Journal of Science and Technology

The present study describes the degradation of tenoforvir disoproxil fumarate (teno) under different prescribed stress conditions (hydrolysis, oxidation, dry and… Continue reading Development and validation of a stability-indicating lc method for the determination of tenofovir disoproxil fumarate in pharmaceutical formulation

DJ Tognarelli

Development and Validation of LC Method for the Simultaneous Estimation of Rosuvastatin Calcium and Olmesartan Medoxomil in Pharmaceutical Dosage Form

2014 / International Journal of ChemTech Research

A simple, fast, and precise reverse phase, isocratic HPLC method was developed for the separation and quantification of Rosuvastatin calcium… Continue reading Development and Validation of LC Method for the Simultaneous Estimation of Rosuvastatin Calcium and Olmesartan Medoxomil in Pharmaceutical Dosage Form

DJ Tognarelli

DEVELOPMENT AND VALIDATION OF LC METHOD FOR THE SIMULTANEOUS ESTIMATION OF ROSIGLITAZONE MALEATE AND GLIMEPIRIDE IN PHARMACEUTICAL DOSAGE FORM

2012 / Malaysian Journal of Pharmaceutical Sciences

A simple, precise and accurate high performance liquid chromatography (HPLC) method was developed for simultaneous quantitative determination of rosiglitazone maleate… Continue reading DEVELOPMENT AND VALIDATION OF LC METHOD FOR THE SIMULTANEOUS ESTIMATION OF ROSIGLITAZONE MALEATE AND GLIMEPIRIDE IN PHARMACEUTICAL DOSAGE FORM

DJ Tognarelli

DEVELOPMENT AND VALIDATION OF A RP – LC METHOD FOR DISSOLUTION TEST OF EFAVIRENZ TABLETS AND ITS APPLICATION TO DRUG QUALITY CONTROL STUDIES

2013 / Asian Journal of Pharmaceutical and Clinical Research

A liquid chromatographic method is developed to evaluate a new dissolution profile of Efavirenz in tablet dosage form. The dissolution… Continue reading DEVELOPMENT AND VALIDATION OF A RP – LC METHOD FOR DISSOLUTION TEST OF EFAVIRENZ TABLETS AND ITS APPLICATION TO DRUG QUALITY CONTROL STUDIES

DJ Tognarelli

A validated stability indicating RP-HPLC method for valganciclovir, identification and characterization of forced degradation products of valganciclovir using LC-MS/MS

2014 / Acta Chromatographica

The objective of the present study was to report the stability of novel antiviral drug, valganciclovir based on the information… Continue reading A validated stability indicating RP-HPLC method for valganciclovir, identification and characterization of forced degradation products of valganciclovir using LC-MS/MS

DJ Tognarelli
Page 105 of 481