Veterinary Drugs Control Act Article 3-1
The term "preparations" as used in this Act refers to veterinary drugs which are processed and compounded from raw materials into a specific pharmaceutical form and dosage.Categories of preparations shall be promulgated by the central competent authority.Preparations are classified into veterinary drugs to be prescribed by veterinarians (or veterinary assistants) and non-prescription veterinary drugs.Regarding prescription drugs specified in the preceding Paragraph, their categories, terms of purchase and sale, methods of use, information to be included on prescriptions, storage procedures, record-keeping requirements for sales, and other matters requiring compliance shall be prescribed by the central competent authority.
中文原文 動物用藥品管理法第3-1條
本法所稱製劑，指以原料藥經加工調製，製成一定劑型及劑量之動物用藥品。
製劑之劑型種類，由中央主管機關公告之。
製劑分為獸醫師（佐）處方藥品及非處方藥品。
前項獸醫師（佐）處方藥品之品目、買賣條件、使用方式、處方箋記載事項、保存、販賣應記錄資料及其他應遵行事項之辦法，由中央主管機關定之。
製劑之劑型種類，由中央主管機關公告之。
製劑分為獸醫師（佐）處方藥品及非處方藥品。
前項獸醫師（佐）處方藥品之品目、買賣條件、使用方式、處方箋記載事項、保存、販賣應記錄資料及其他應遵行事項之辦法，由中央主管機關定之。