Development and validation of stability indicating rp-uplc assay method for the determination of lacosamide and quetiapine fumarate in bulk and tablet dosage forms - Egyptian Knowledge Bank - troweb

101878

Development and validation of stability indicating rp-uplc assay method for the determination of lacosamide and quetiapine fumarate in bulk and tablet dosage forms

Article

Last updated: 04 Jan 2025

Overview Similar Items

Article

Development and Validation of UV Spectroscopic and RPHPLC Method for Determination of Levetiracetam in Bulk and Combined Dosage Form

Article

STABILITY INDICATING HPLC METHOD FOR THE DETERMINATION OF AGOMELATINE INPLASMA AND TABLET FORMULATION

Article

STABILITY – INDICATING SPECTROPHOTOMETRIC METHODS FOR DETERMINATION OF LAMOTRIGINE IN PURE FORM AND PHARMACEUTICAL PREPARATIONS

Article

STABILITY-INDICATING HPLC AND UV SPECTROPHOTOMETRIC DETERMINATION OF SOFOSBUVIR IN PURE FORM AND TABLETS

Article

Stability-Indicating Spectrophotometric Methods for Determination of Milnacipran HCl and Duloxetine HCl in Bulk Drug and Pharmaceutical Formulations

Article

Method Development and Validation for Estimation of Vonoprazan By RP-HPLC Method In Bulk and Tablets Dosage Form

Article

ANALYTICAL METHOD DEVELOPMENT AND VALIDATION FOR SIMULTANEOUS DETERMINATION OF CABOTEGRAVIR AND RILPIVIRINE USING RP-HPLC

Article

Development and Validation of Stability-Indicating GC-MS Method for Simultaneous Determination of Lumefantrine and Artemether

Article

Stability Indicating Assay Method of Metformin, Linagliptin and Empagliflozinin Pharmaceutical Dosage Form by HPLC Method

Article

Stability Indicating Reverse Phase High-performance Liquid Chromatographic Determination of Pioglitazone Hydrochloride in Pharmaceuticals and Human Urine