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Abstract The purpose of this study is to apply a triplicate design approach to bioequivalence study of azithromycin following a 500-mg oral dose to 8 subjects,

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Bioequivalence study of two azithromycin formulations in healthy subjects. Setiawati E, Deniati SH, Yunaidi DA, Handayani LR, Harinanto G, Santoso ID, Sari AP

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Bioequivalence Study of Azithromycin Granules in Human by HPLC-MS/MS. REN Jing1,2,LI Ke-jia1,YE Li-ming1,JIANG Xue-hua1*,XIONG

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Quantitative determination of azithromycin in human plasma by liquid spectrometry and its application in a bioequivalence study. Chen BM

Date: 2011-11-08. Azithromycin 250 mg capsules(Eng).doc. Study Synopsis Title Bioequivalence Study of Azithromcycin 250 mg Capsules

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OBJECTIVE To develop a HPLC-MS/MS method for the determination of the concentration of azithromycin in human plasma,and to evaluate the bioequivalence

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Key words: azithromycin; bioequivalence study; HPLC; pharmacokinetics. Introduction. Bioequivalence of the two formulations of the same drug comprises

Objective: To study the bioequivalence and relative bioavailability of azithromycin for suspension. Method: A single oral dose(500 mg of test or reference) were


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