Development and validation of stability-indicating liquid chromatographic method for the quantitative determination of oxcarbazepine in tablet dosage forms
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Publisher
EManuscript Technologies
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General Pharmacology, Toxicology and Pharmaceutics
Cited by 8 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. Analysis of Carbamazepine, Oxcarbazepine, Their Impurities, and Non-Labeled Interfering Substances by Stability-indicating UPLC/MS/MS Method: Studying the Method’s Greenness Profile;Chromatographia;2018-10-09
2. Comparative effect of divided doses of adult solid and liquid oral formulations of antiepileptic drugs in the management of pediatric epilepsy;Journal of Pharmacology and Pharmacotherapeutics;2017
3. The use of separation techniques in the analysis of some antiepileptic drugs: A critical review;Journal of Liquid Chromatography & Related Technologies;2016-11-07
4. SPECTROPHOTOMETRIC AND SPECTROFLUORIMETRIC DETERMINATION OF OXCARBAZEPINE IN PURE FORM AND PHARMACEUTICAL PREPARATION;International journal of pharmaceutical sciences and research;2014-09-01
5. Development and validation of a stability-indicating RP-LC method for the estimation of process-related impurities and degradation products of oxcarbazepine in pharmaceutical formulation;Acta Chromatographica;2014-06
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