本計劃於民國86年9月至87年6月委託台北市政府衛生局、高雄市政府衛生局及全省各縣市衛生局到各公私立醫院或藥局抽樣Amoxicillin膠囊製劑之檢體共87件,包括國產品86件及輸入品1件。依據美國藥典第23版所記載之高效液相層析法予以檢驗。結果含量約符合藥典規定之合格範圍(90%~120%),合格率為100%。
In order to assess the potency of amoxicillin products, eighty seven samples (86 domestic, 1 imported) were sampled from different counties and cities throughout Taiwan from September 1997 to June 1998. All samples were determined by a high performance liquid chromatographic method as described in the United States Pharmacopeia and Chinese Pharmacopeia as well. The results showed that all samples met the potency requirement of the government regulation (90-120%).
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