Pharmacokinetics of valpromide after oral administration of a solution and a tablet to healthy volunteers

Abstract

The pharmacokinetics of valpromide, a primary amide of valproic acid, was investigated in 6 healthy, adult male volunteers, each of whom was given 900 mg as a marketed, enteric-coated tablet and a solution. Valpromide was biotransformed to valproic acid after the administration of the tablet and the solution with a bioavailability of 0.79±0.24 and 0.77±0.12… (More)
DOI: 10.1007/BF00549603

Topics

1 Figure or Table

Cite this paper

@article{Bialer1984PharmacokineticsOV, title={Pharmacokinetics of valpromide after oral administration of a solution and a tablet to healthy volunteers}, author={Meir Bialer and Alan Rubinstein and Itamar Raz and Oded Abramsky}, journal={European Journal of Clinical Pharmacology}, year={1984}, volume={27}, pages={501-503} }