I. Landing in official website, State Administration of Pharmaceutical Products.
First, you need to open the official website of the State Administration of Medical Supplies. This website is the authoritative platform for the official release of drug information, including drug filing, registration, approval and other related information.
Two, enter the drug record query system
On the homepage of official website, there is usually a "drug inquiry" or similar entrance. Click to enter and select the "Drug Filing Inquiry" system.
Third, enter the query conditions.
In the drug filing inquiry system, it is necessary to input the drug name, manufacturer, record number and other related information as the inquiry conditions. If you know the specific record number, you can directly enter it for query; If you are not sure about the record number, you can inquire through the name of the drug or the manufacturer.
Fourth, get the query results.
After entering the query criteria, the system will return the relevant drug filing information. If the query is successful, you can see the drug record number, drug name, manufacturer, filing date and other detailed information.
Verb (abbreviation for verb) verifies the accuracy of information.
After checking the drug record number, it is suggested to further verify the accuracy of the information. You can compare the information on the drug package with the query results, or contact the drug manufacturer for confirmation.
To sum up:
To query the drug record number, you need to visit the official website of the State Medical Supplies Supervision Administration, enter the drug record number query system, enter the query conditions such as drug name, manufacturer or record number, obtain the query results, and verify the accuracy of the information. Drug number is an important symbol and basic information of drug legality, which is of great significance to ensure the safety of public drug use.
Legal basis:
People's Republic of China (PRC) Drug Administration Law
Article 5 provides that:
The state implements the system of drug marketing license holders. The holder of the drug marketing license is responsible for the safety, effectiveness and quality controllability of the whole process of drug research and development, production, management and use according to law.
People's Republic of China (PRC) Drug Administration Law
Article 78 provides that:
For listed drugs, the drug supervision and administration department of the State Council shall organize technicians such as pharmacy and medicine to conduct post-marketing evaluation. The problems found in the evaluation should be dealt with in time.