To investigate the effect of elastic recovery on the release of bupropion hydrochloride sustained-release tablets.

考查非他酮缓释片压片后强度的变化对释度的影响。

After reiewing the issues raised in the petition, FDA determined that its standards for approal of the generic drug application for bupropion are appropriate.

FDA审查请愿书中的问题后确认，非他酮仿制药申请的标是恰当的。