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Sci. Pharm.
Volume 78
Issue 3
10.3797/scipharm.cespt.8.PPAT12
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Scientia Pharmaceutica is published by MDPI from Volume 84 Issue 3 (2016). Previous articles were published by another publisher in Open Access under a CC-BY (or CC-BY-NC-ND) licence, and they are hosted by MDPI on mdpi.com as a courtesy and upon agreement with Austrian Pharmaceutical Society (Österreichische Pharmazeutische Gesellschaft, ÖPhG).
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Conference Report

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

by
I. KOCIC
*,
I. HOMSEK
and
M. DACEVIC
R&D Institute, Galenika ad, Belgrade, Serbia
*
Author to whom correspondence should be addressed.
Sci. Pharm. 2010, 78(3), 701; https://doi.org/10.3797/scipharm.cespt.8.PPAT12
Submission received: 12 July 2010 / Accepted: 12 July 2010 / Published: 12 July 2010
Versions Notes

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]. [...]

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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. https://doi.org/10.3797/scipharm.cespt.8.PPAT12

AMA Style

KOCIC I, HOMSEK I, DACEVIC M. Application of Experimental Design for Screening Study of Dissolution Test Conditions: Levothyroxine Sodium Immediate-Release Tablets. Scientia Pharmaceutica. 2010; 78(3):701. https://doi.org/10.3797/scipharm.cespt.8.PPAT12

Chicago/Turabian Style

KOCIC, I., I. HOMSEK, and M. DACEVIC. 2010. "Application of Experimental Design for Screening Study of Dissolution Test Conditions: Levothyroxine Sodium Immediate-Release Tablets" Scientia Pharmaceutica 78, no. 3: 701. https://doi.org/10.3797/scipharm.cespt.8.PPAT12

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