Validated stability indicating chromatographic method for determination of baricitinib and its degradation products in their tablet dosage form: Implementation to content uniformity and in vitro dissolution studies-Reference-Cited by-同舟云学术

Validated stability indicating chromatographic method for determination of baricitinib and its degradation products in their tablet dosage form: Implementation to content uniformity and in vitro dissolution studies

Published:2023-03 Issue:2 Volume:81 Page:267-283
ISSN:0003-4509
Container-title:Annales Pharmaceutiques Françaises
language:en
Short-container-title:Annales Pharmaceutiques Françaises

Author:

Mohamed M.A.^ORCID

Publisher

Elsevier BV

Subject

Pharmaceutical Science,Pharmacology

Reference13 articles.

1. Expanded access programs, compassionate drug use, and emergency use authorizations during the COVID-19 pandemic;Rizk;Drug Discovery Today,2021

2. Baricitinib, methotrexate, or combination in patients with rheumatoid arthritis and no or limited p1r00ior disease-modifying antirheumatic drug treatment;Fleischmann;Arthritis & Rheumatology,2017

3. British Pharmacopoeia Stationary Office, Medicines and Healthcare Products Regulatory Agency. 2022; London, Vol. II.

4. The United States Pharmacopoeia 43 Revision, NF 38. 2022; the United States Pharmacopoeia Convention Inc.

5. Development and validation of a stability indicating related substances of baricitinib by RP-HPLC and its degradation;Mohan;Int J Manag Hum,2019

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