Stability-Indicating Assay, Dissolution, and Content Uniformity of Sodium Levothyroxine in Tablets
Author:
Publisher
Elsevier BV
Subject
Pharmaceutical Science
Reference17 articles.
1. The United States Pharmacopeia,1980
2. Reversed-Phase High-Performance Liquid Chromatographic Analysis of Liothyronine Sodium and Levothyroxine Sodium in Tablet Formulations: Preliminary Studies on Dissolution and Content Uniformity
3. Catalytic detection principle for high-performance liquid chromatography: Determination of enantiomeric iodinated thyronines in blood serum
4. The Separation and Determination of Liothyronine and Levothyroxine in Tablets by Reversed-Phase High Performance Liquid Chromatography
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1. Potency and Powder X-ray Diffraction (PXRD) Evaluation of Levothyroxine Sodium Tablets under Ambient, Accelerated, and Stressed Conditions;Pharmaceuticals;2023-12-27
2. Analytical Methods for the Estimation of Levothyroxine and Levothyroxine Sodium in Pharmaceutical Formulations – A Review;International Journal of Pharmaceutical Sciences and Nanotechnology(IJPSN);2023-11-15
3. A derivative UV spectrophotometric method for the determination of levothyroxine sodium in tablets;Journal of Analytical Chemistry;2013-05-29
4. Development and application of a validated HPLC method for the analysis of dissolution samples of levothyroxine sodium drug products;Journal of Pharmaceutical and Biomedical Analysis;2011-02
5. Stability indicating validated HPLC method for quantification of levothyroxine with eight degradation peaks in the presence of excipients;International Journal of Pharmaceutics;2008-08
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