首页> 外国专利> A method for the preparation of a solid farcºutico preparado (Machine-translation by Google Translate, not legally binding)

A method for the preparation of a solid farcºutico preparado (Machine-translation by Google Translate, not legally binding)

机译:一种制备固体farcºutico制备品的方法(通过Google Translate进行机器翻译,不具有法律约束力)

摘要

A method for the preparation of a solid pharmaceutical preparation containing water-dispersible grains of one or more salts, other than embonate, of the formula **(See formula)** where R1 is a hydrogen, chlorine or bromine atom or a methyl or nitro group; R2 is a hydrogen, fluorine, chlorine or bromine atom or a methyl group; and A- is an anionic equivalent of a pharmaceutically acceptable acid that is chosen so that the salt has a solubility in water of less than 2% w/v at 200ºC, characterized in that 1 to 10 parts by weight of one or more soluble embonates are they mix with 80 to 95 parts of said water dispersible granules. (Machine-translation by Google Translate, not legally binding)
机译:一种制备固体药物制剂的方法,该药物制剂包含一种或多种除**的血栓以外的盐的水分散性颗粒,其中R1是氢,氯或溴原子或甲基或硝基R 2是氢,氟,氯或溴原子或甲基; A-是药学上可接受的酸的阴离子当量,其被选择为使得该盐在200℃下在水中的溶解度小于2%w / v,其特征在于1至10重量份的一种或多种可溶的磺酸盐它们是否与80至95份上述水分散性颗粒混合。 (通过Google翻译进行机器翻译,没有法律约束力)

著录项

  • 公开/公告号ES254939A1

    专利类型

  • 公开/公告日1960-06-16

    原文格式PDF

  • 申请/专利权人 THE WELCOME FOUNDATION LIMITED;

    申请/专利号ES19600254939

  • 发明设计人

    申请日1960-01-12

  • 分类号1A61KA;

  • 国家 ES

  • 入库时间 2022-08-23 19:33:23

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