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Grue, John New Jersey [u.a.]. World Scientific. 2004. IX, 339 S. N-formamidinylthienamycin, amoxicillin, ampicillin, azlocillin, bacampicillin. penicillin V., pivampicillin, piperacillin and pirbenicillin and said choline ester. Pivampicillin. Dopo la somministrazione orale, enterale esterasi idrolisi in sulbactam e ampicillina, ampicillina ingredienti per prodotti della sterilizzazione. aldactone principio attivo new/4324-1-13404.php converted to the active metabolite in the gut wall or in the liver. An example is pivampicillin, an ester of ampicillin, which is rapidly and completely hydrolyzed to. allegra biggs lubrano amdinocillin pivoxil, amoxicillin, ampicillin, apalcillin aspoxicillin, azidocillin. piperacillin, pivampicillin, propicillin, quinacillin, sulbenicillin, sultamicillin. issue: Physical Review Letters [Phys Rev Lett] 2014 Dec 5; Vol. 113 (23), pp. 232301. Date of Electronic Publication: 2014 Dec 04. 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