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23:24
最后更新: 2018-02-13
使用频率: 1
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115%.
the guideline on excipients in the dossier for application for marketing authorisation of a medicinal product (emea/ chmp/ qwp/ 396951/ 2006) and the above mentioned guideline (chmp/ 463/ 00) indicate which excipients and information should appear in the labelling.