Development and Validation of RP-HPLC Method for Dissolution Drug Release of Dimethyl Fumarate Delayed Release Capsules
Author:
Affiliation:
1. Department of chemistry, Faculty of Basic Science, AKS University, Sherganj, Panna Road, Satna-485001, MP, India
Publisher
Informa UK Limited
Link
https://www.tandfonline.com/doi/pdf/10.1080/22297928.2021.1914723
Reference41 articles.
1. Patient information, Techfidera, (2017). Highlights of prescribing information, BiogenInc, Cambridge [Approved by the U. S. Food and Drug Administration, Revised: 1/2017]. Available at: https://www.accessdata.fda.gov/drugsatfda_docs/label/2017/204063s017lbl.pdf
2. Australian Public Assessment Report for Dimethyl Fumarate. Available at: https://www.tga.gov.au/sites/default/files/auspar-dimethyl-fumarate-131022.pdf
3. STABILITY INDICATING RP-HPLC ASSAY METHOD FOR ESTIMATION OF DIMETHYL FUMARATE IN BULK AND CAPSULES
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