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Autor:
Névine Zariffa, Bernard E. Ilson, David E. Martin, David Lundberg, Steve Boike, Duane A. Boyle, Diane K. Jorkasky, John Jushchyshyn, David Tenero
Publikováno v:
Biopharmaceutics & Drug Disposition. 19:351-356
Eighteen healthy males received a single 300 mg oral dose of eprosartan as the commercial wet granulation formulation under fasting conditions and following a high-fat breakfast and a single 20 mg intravenous (i.v.) dose. The pharmacokinetics of i.v.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::139bb8e8ec7eabf5e0f713858362832a
https://doi.org/10.1002/(sici)1099-081x(199809)19:6<351::aid-bdd115>3.0.co
https://doi.org/10.1002/(sici)1099-081x(199809)19:6<351::aid-bdd115>3.0.co
