Bioequivalence study as component of the pharmaceutical development for the Azithromycin capsules 500 mg.
Pharmaceutical development is carried out and the medicine Azithromycin, capsules 500 mg introduced into production. The medicine is equivalent to the reference preparation, which was registered in Ukraine, in accordance with the requirements of the Investigation of Bioavailability and Bioequivalence.
2. Regulation 42-7.1.2005. Guidance on quality. Research on bioavailability and bioequivalence.
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4. Shklyaev S.A., Tsurkan O.O., Kolyadych O.P., Kulikova O.O. // Pharmaceutical Journal. - 2011. - No. 1 - P. 64-68.
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