Stability-Indicating Assay, Dissolution, and Content Uniformity of Sodium Levothyroxine in Tablets

作者: Steven L. Richheimer , Tahani M. Amer

DOI: 10.1002/JPS.2600721129

关键词:

摘要: A reverse-phase high-performance liquid chromatographic (HPLC) method for determining sodium levothyroxine in tablet formulations is described. The was extracted from tablets using a mobile phase consisting of 60% acetonitrile and 40% aqueous buffer. After centrifugation 200 μl the solution chromatographed on 10-μm C18 column. gave accurate results when tested against USP method, by standard additions spiked-placebo method. can also be used to determine content uniformity dissolution tablets.

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