Drug packaging materials and the data field of packaging on the application form should comply with the following regulations:1.The quantity, materials and types of the drug packaging should be specified;2.Except for oral nutrient liquids, all bottled solutions for oral internal use and syrups, shall not be packed in ampoule. The volume should be indicated on each bottle; and3.The unit recorded in the data field of packaging on the application form should be identical to the unit dosage form of the formula.The maximum package size for drugs should follow the standards in the Table of Maximum Package Size. If there are any special purposes for the maximum package size, the purposes should be stated on the packaging. For common pharmaceutical preparations, the minimum package size is the two-day dose for an adult. For syrup containing codeine (phosphate) as an instruction drug, the maximum package size is the three-day dose. Tablets or capsules containing ephedrine or pseudoephedrine should only be packed in aluminium blister foils and boxes. For instruction drugs, the maximum package size is the seven-day dose for an adult. For drugs for the cold, fever, pain relief and for the cough liquid, the package size should be between one single adult dose and 4000 ml. The restrictions do not apply to sickness drugs and pesticides.Please see Appendix 1 for the Table of Maximum Package Size as mentioned above.In the situation where the packaging is over its maximum package size, an application to change the registration should be made by providing documents of purchasing orders from health care providers or academic institutes. The application for changes does not apply to instruction drugs containing ephedrine or pseudoephedrine.Appendix1：Maximum Drug Package Size Dosage.pdf