VALIDATION OF UV-SPECTROMETRY ASSAY METHOD FOR DISSOLUTION PROFILE TEST FOR MOXIFLOXACINE TABLETS

Validation of UV-spectrometry assay method for dissolution profile test for levofloxacine tablets was carried out. The evaluated validation characteristics were: specificity, linearity, accuracy, precision, and analytical range. It was shown than main validation characteristics meet the Russian Stat...

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Bibliographic Details
Main Authors:	L. A. Menshikova, A. A. Lvova, I. E. Shohin, Yu. E. Boldina, T. N. Komarov, Yu. V. Medvedev
Format:	Article
Language:	Russian
Published:	LLC Center of Pharmaceutical Analytics (LLC «CPHA») 2019-01-01
Series:	Разработка и регистрация лекарственных средств
Subjects:	moxifloxacine validation uv-spectrophotometry dissolution profile test
Online Access:	https://www.pharmjournal.ru/jour/article/view/89

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