Bioequivalence trial of Diclofenac sodium tablets: Effects of Eudragit and tablet preparation, formulation characterization, release profiles, and bioavailability measurements

Author:

Kecman Sanja,Jokanovic Milan

Publisher

Centre for Evaluation in Education and Science (CEON/CEES)

Subject

Applied Mathematics

Reference21 articles.

1. Popović J, Mikov M, Sabo A, Jakovljević V. Evaluation of statistical power function for various diclofenac bioequivalence trials with different subject numbers. Eur J Drug Metabol Pharmacokinet 2009; 34: 85.;

2. Ali H, Shoaib MH, Zafar F, et al. Pharmacokinetic and bioequivalence studies of immediate release diclofenac potassium tablets (50 mg) in healthy volunteers. Pak J Pharm Sci 2016; 29: 1671-79.;

3. In-vitro/In-vivo correlation for extended-release oral dosage forms. Stimuli to the revision process. The United States Pharmacopeia Convention Inc, 1988; 4160.;

4. PMA's Joint Committee on Bioavailability. The role of dissolution testing in drug quality, bioavailability and bioequivalence testing. Pharm Technol 1985; 9: 62-6.;

5. Welling PG. Pharmacokinetics: processes and mathematics. Washington. DC: American Chemical Society, 1986.;

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