药品包装规范（Drug package specification）.docVIP

药品包装规范（Drug package specification） According to the order of the State Drug Administration No. twenty-third, for the packaging and label management to further strengthen and standardize the drug, ensure drug packaging, label and manual management regulations (Provisional) implementation, these rules are formulated. General requirement First, drug packages and labels must be printed according to the requirements prescribed by the State Administration of drug supervision, and their words and designs shall not be added to any content that has not been examined and approved. The package of medicine is divided into inner packing and outer packing. The contents of pharmaceutical packages and labels shall not exceed the content prescribed by the Drug Administration approved by the State Drug administration. Two, drug packaging, label printing content of products of expression should be accurate, in addition to express safe and rational use of words, not all with inappropriate advertising text and logos, such as national drug, protection of varieties of traditional Chinese medicine, GMP certification, imported raw, producer and produced and award-winning products, quality of the insurance company insurance and public reimbursement and modern science and technology, rare medicinal herbs. The drug name shall be used on the package and label before it is approved by the State Drug administration. Brand name and general name should not write, branch. After the commodity name has been registered, it shall still be in conformity with the principle of commodity name management. The proportion of words used in common name and trade name shall not be less than 1:2 (area). The generic name should be of the same size, without parentheses. A registered trademark that has not been approved by the State Administration of drug administration as a commodity name may be printed in the upper left corner or upper right corner of the package label, and its typeface shall not be larger than the