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USE OF DISSOLUTION TEST FOR EVALUATION OF PHARMACEUTICAL EQUIVALENCE OF ATORVASTATIN GENERICS

This article shows the results of a study of pharmaceutical equivalence of atorvastatin generics using Dissolution test. A significant difference in the intensity of atorvastatin release from tablets from different manufacturers has been established. From 10 to 97% of atorvastatin was released from...

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Principais autores: O. V. Druzhininskaya, I. E. Smekhova
Formato: Artigo
Idioma:Russo
Publicado em: LLC Center of Pharmaceutical Analytics (LLC «CPHA») 2019-01-01
coleção:Разработка и регистрация лекарственных средств
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Acesso em linha:https://www.pharmjournal.ru/jour/article/view/561
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