The first part includes medicinal materials and decoction pieces, vegetable oil and extracts, prescription preparations and single-flavor preparations;
The second part includes chemicals, antibiotics, biochemical drugs and radioactive drugs;
Three collections of biological products;
Four general principles of collection and loading, including: general principles of preparations, inspection methods, guiding principles, general principles related to reference substances and test solutions, pharmaceutical excipients, etc.
China Pharmacopoeia, the abbreviation of People's Republic of China (PRC) Pharmacopoeia, was published by China Medical Science and Technology Press on June 5, 20 15, and was created by the State Pharmacopoeia Committee.
Extended data
1, as a code to ensure the quality of drugs in China, this edition of Pharmacopoeia focuses on solving outstanding problems that restrict the quality and safety of drugs and improving the quality control level of drug standards on the basis of maintaining scientificity, advancement, standardization and authority.
Fully drawing lessons from international advanced technology and experience objectively reflects the current level of China's pharmaceutical industry, clinical use and inspection technology, which will certainly play a positive and important role in improving drug quality, and will further expand and enhance the positive influence of China's Pharmacopoeia in the world.
2, where the varieties of China Pharmacopoeia, since the date of implementation, originally contained in the Calendar Pharmacopoeia, drug standards promulgated by the Ministry of Health, new drug conversion standards promulgated by the State Food and Drug Administration of the United States and local standards rose to national standards, the drug standards of the same variety shall be abolished at the same time.
3. If the drug registration standard does not meet the relevant requirements of China Pharmacopoeia, the drug production enterprise shall submit a supplementary application in accordance with the relevant provisions of the Measures for the Administration of Drug Registration. If the drug registration standard contains more inspection items than those specified in China Pharmacopoeia or the quality index is higher than that required by China Pharmacopoeia, the corresponding items and indicators in the original standard shall be implemented on the basis of implementing China Pharmacopoeia.
4. For varieties not listed in the China Pharmacopoeia, their quality standards shall be implemented according to the relevant requirements of the same variety in the China Pharmacopoeia, and the specifications shall be implemented according to the original approval documents.
Baidu Encyclopedia-China People's Pharmacopoeia