Development and Validation of a Stability-Indicating HPLC Method for the Assay of Carvedilol in Pure and Tablet Dosage Forms
Author:
Affiliation:
1. Baqai Institute of Pharmaceutical Sciences, Baqai Medical University, 51, Deh Tor, Toll Plaza, Super Highway, Gadap Road, Karachi-74600, Pakistan
2. Getz Pharma (Pvt.) Limited, Korangi Industrial Area, Karachi-74900, Pakistan
Publisher
Bentham Science Publishers Ltd.
Subject
Pharmaceutical Science,Molecular Medicine,Biochemistry,Biophysics
Cited by 12 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Analytical Technique for Carvedilol and Ivabradine determination from pure and Pharmaceutical Dosage Forms: A Review;Asian Journal of Pharmaceutical Analysis;2023-06-03
2. New ecological first derivative synchronous spectrofluorimetric method for simultaneous quantification of carvedilol and ivabradine in tablets;Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy;2023-03
3. Functional group-specific multilateral derivatization cum extraction method for simultaneous quantification of genotoxic impurities in carvedilol phosphate drug using GC-MS and their toxicity assessments;Journal of Pharmaceutical and Biomedical Analysis;2022-10
4. Quantification of rosmarinic acid from different plant species of lower Himalayan region and expression analysis of underlying L‐Phenylalanine pathway;Physiologia Plantarum;2022-08-31
5. Simultaneous Determination of Carvedilol and its Impurities in Tablets by High Performance Liquid Chromatography;Indian Journal of Pharmaceutical Sciences;2022
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