Degradation of ondansetron: Isolation and characterization impurity D ondansetron as A candidate reference standard impurity in drug-Reference-Cited by-同舟云学术

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Degradation of ondansetron: Isolation and characterization impurity D ondansetron as A candidate reference standard impurity in drug

Published:2020 Issue: Volume: Page:
ISSN:0094-243X
Container-title:PROCEEDINGS OF THE 5TH INTERNATIONAL SYMPOSIUM ON CURRENT PROGRESS IN MATHEMATICS AND SCIENCES (ISCPMS2019)
language:
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Author:

Kristiana E.,Saefumillah A.,Budianto E.

Publisher

AIP Publishing

Link

http://aip.scitation.org/doi/pdf/10.1063/5.0010657

Reference8 articles.

1. Review of analytical methodologies for the determination of 5-HT3 receptor antagonists

2. Selective separation and characterization of the stress degradation products of ondansetron hydrochloride by liquid chromatography with quadrupole time-of-flight mass spectrometry

3. United States Pharmacopeial, U. S. Pharmacopeia National Formulary 2019: UPS42-NF37 (United States Pharmacopeial, Maryland, 2019).

4. Toxicological overview of impurities in pharmaceutical products☆

5. Critical review of reports on impurity and degradation product profiling in the last decade

Cited by 1 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. Determination of N-nitrosodimethyl amine impurity in valsartan by HPLC and LC-MS/MS methods;Chinese Journal of Analytical Chemistry;2022-11

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