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第一绦本细则依管理麻醉药品暂行条例(以下简称本条例)第十七条之规定订定之。第二条本条例所称麻醉药品之输入,系指麻醉药品供应机构依本条例第五条至第七条之规定,向国外采购运至本国口岸进口而言。第三条本条例所称麻醉药品之制造,系指麻醉药品之提炼、精制及其制剂之调制。第四条本条例所称麻醉药品之制剂,系指麻醉药品之酊剂、锭剂、安瓿等,及含吗啡在千分之二以上或含可卡因在千分之一以上之其它制剂。
The First Article of this Article shall be formulated in accordance with the provisions of Article 17 of the Provisional Regulations on the Administration of Narcotic Drugs (hereinafter referred to as the “Regulations”). Article 2 The importation of narcotic drugs as mentioned in these Regulations refers to the narcotic drug supply agencies that, in accordance with the provisions of Articles 5 to 7 of these Regulations, procure the goods from abroad for import to their own ports of entry. Article 3 The manufacture of narcotic drugs as mentioned in these Regulations refers to the refining, refining and preparation of narcotic drugs. Article 4 The formulation of narcotic drugs as mentioned in these Regulations refers to tinctures, lozenges, ampoules and the like of narcotic drugs, and other preparations containing more than two per thousand morphine or more than one thousandth of a cocaine.