Batch results from in-process monitoring, content uniformity, dissolution, and other tests are consistent with the passing retest results. 批分析结果从中间控制、产品均一性、产品分散性和其他检测均与复测结果相吻合。
With the exception of one batch, all batches tested have met the USP XXII requirements for dissolution test in the case of the dissolution test. 在体外溶出实验中除一批外,其余各批均符合英国药典和USPXXII的溶出要求。