SCIENCE4HEALTH 2016. Клинические и теоретические аспекты современной медицины : материалы VII Международной научной конференции. Москва, 12–15 апреля 2016 г..
РУДН.
2016.
С. 30-31
The study was aimed to assess the equivalence of valsartan tablets of different manufacturers using in vitro dissolution study. Materials and methods: The dissolution was carried out using the apparatus II.Results: A similarity factor (f2) was employed. Samples with pH 1.2 and 4.5 showed the value more than 50%. Samples in pH 6.8 attained more than 85% dissolution within 15 minutes. Сonclusions: Studied tablets are equivalent to original drug.