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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Bibliographic Details
Main Authors: S. A. Altynbekov (Author), G. A. Dzholdygulov (Author), V. N. Seryakov (Author), Y. M. Budach (Author), O. E. Kurilo (Author), N. I. Kuznetsova (Author)
Format: Book
Published: LLC "Publisher OKI", 2013-09-01T00:00:00Z.
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3rd Floor Main Library

Holdings details from 3rd Floor Main Library
Call Number: A1234.567
Copy 1 Available