A UPLC method development and validation study of Upadacitinib and its impurities in extended – release oral tablet dosage forms

Author:

Nimmagadda Rajya Lakshmi,Gummadi Sowjanya

Publisher

Elsevier BV

Reference14 articles.

1. Europe PMC. URL: https://europepmc.org/article/NBK/nbk572088. Accessed on [March 30, 2023]

2. European Medicines agency. URL: https://www.ema.europa.eu/en/medicines/human/EPAR/rinvoq. Accessed on [March 30, 2023].

3. Related substances method development and validation of Axitinib, Zanubrutinib and Upadacitinib using RP-HPLC and its degradation products were characterized by using LC-MS/MS;Ibrahim;Int J Pharm Investig,2023

4. Quantification of the Janus kinase 1 inhibitor Upadacitinib in human plasma by LC-MS/MS;Martens-Lobenhoffer;J Chromatogr B,2022

5. Quantification of an anti-rheumatic agent: Upadacitinib in biological fluid (plasma) by LC-MS/MS;Venkateswara Rao;J Pharm Negat Results,2022

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