ABSTRACT

Fexofenadine Hydrochloride is indicated to relieve signs and symptoms of related to seasonal allergic rhinitis. The aim of the present study is to establish the pharmaceutical equivalence of different brands of Fexofenadine Hydrochloride 120 mg tablets available in the market. The quality control tests performed are weight variation, friability, hardness, disintegration and invitro dissolution studies. In-Vitro dissolution studies of Fexofenadine Hydrochloride 120 mgg tablets were carried out in 6.8 pH phosphate buffer. Two samples are compared with the Innovator product. During the evaluation no major difference was noticed in weight variation, friability, hardness, disintegration and in dissolution between the two market products and the innovator product. Keywords: Fexofenadine Hydrochloride, weight variation, friability & invitro dissolution studies
Publication date: 01/08/2026

https://www.ijbpas.com/pdf/2026/August/MS_IJBPAS_2026_10350.pdf

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https://doi.org/10.31032/IJBPAS/2026/15.8.10350