Enforcement Rules of Veterinary Drugs Control Act Article 10
The recalled veterinary drugs and the inventory, whose veterinary drug licenses are annulled in accordance with Article 30 of the Act, shall be handled according to the following regulations:10.1 The inventory of qualified veterinary drugs must not be sold until the municipal or county (city) competent authority check thoroughly the amount and affixes the “ veterinary drug checkup stamp ” to the label or the obvious place of the packaging of every bottle.10.2 The recalled veterinary drugs and the inventory of counterfeit, banned or substandard veterinary drugs shall be sealed their final products, bulks, raw materials, labels and package inserts by the municipal or county (city) competent authority, and dealt with them in accordance with the Act.
中文原文 動物用藥品管理法施行細則第10條
經依本法第三十條規定廢止有關許可證之動物用藥品製造業者或輸入業者，其動物用藥品及其已在市面待出售限期收回者，應依下列規定處理之：
一、製造或輸入合於規定之動物用藥品，應由直轄巿或縣（巿）主管機關清查該業者庫存數量，並於每瓶藥品標籤或包裝上之明顯處，加蓋「動物用藥品清查章」後，始准出售。
二、經查驗為動物用偽藥、禁藥、劣藥者，應由直轄巿或縣（巿）主管機關將其成品、半成品、原料、標籤、仿單等予以封存，分別依本法處理之。
一、製造或輸入合於規定之動物用藥品，應由直轄巿或縣（巿）主管機關清查該業者庫存數量，並於每瓶藥品標籤或包裝上之明顯處，加蓋「動物用藥品清查章」後，始准出售。
二、經查驗為動物用偽藥、禁藥、劣藥者，應由直轄巿或縣（巿）主管機關將其成品、半成品、原料、標籤、仿單等予以封存，分別依本法處理之。