Evaluation of bioequivalence of two tablet forms of lisinopril in healthy volunteers
Under cross, single, open, randomized trial with 1 week washout period, with two sequences of 18 volunteers studied bioequivalence coated tablets, two manufacturers of lisinopril (20 mg dose). The concentration of lisinopril in the plasma samples was determined using HPLC with fluorimetric detection...
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| Autors principals: | , , , , , |
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| Format: | Artigo |
| Idioma: | Russo |
| Publicat: |
LLC “Publisher OKI”
2013-09-01
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| Col·lecció: | Фармакокинетика и Фармакодинамика |
| Matèries: | |
| Accés en línia: | https://www.pharmacokinetica.ru/jour/article/view/133 |
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