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Sci. Pharm. 2010, 78(3), 701; doi:10.3797/scipharm.cespt.8.PPAT12

Application of Experimental Design for Screening Study of Dissolution Test Conditions: Levothyroxine Sodium Immediate-Release Tablets

R&D Institute, Galenika ad, Belgrade, Serbia
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Received: 12 July 2010 / Accepted: 12 July 2010 / Published: 12 July 2010
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Abstract

The aim of the study was to present an example of experimental design application to set up the dissolution test conditions for the two immediaterelease products of levothyroxine sodium (L-Na) with proven bioequivalence: the generic product A and the reference product B [1, 2]. [...]
This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. (CC BY 4.0).

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MDPI and ACS Style

KOCIC, I.; HOMSEK, I.; DACEVIC, M. Application of Experimental Design for Screening Study of Dissolution Test Conditions: Levothyroxine Sodium Immediate-Release Tablets. Sci. Pharm. 2010, 78, 701.

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