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Conference Report

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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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

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

APA Style

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

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