How to inquire about the filing information of the US Food and Drug Administration?

1: Enter "State US Food and Drug Administration Data Query" on Baidu, as shown in the following figure:

2. Then the interface appears, and under the column of "Drugs", select the drug type to be queried. This paper takes "domestic drugs" as an example to illustrate.

3. Or you can enter from the official website of the US Food and Drug Administration, and then find the word "drugs" on the right side of the page and click enter.

4: After that, I went to the query page. These three selection boxes are the default options of the system.

5. Make corresponding choices, whether domestic or imported, chemical or traditional Chinese medicine.

6. This paper takes "Gankang" as an example, as shown in the figure, there will be the words "National Medicine Zhunzi" in a more eye-catching position.

7. Enter the letter and number combination of standard Chinese medicine words in the query bar, as shown in the following figure:

8. Click Query, and the information as shown in the figure will appear, which proves that the drug is a regular drug approved by the state. If there is no query, it means it is a fake medicine.

9: Finally, you can click on the information bar to view the detailed information of the drug, such as the manufacturer, address, approval date and a series of information.

Extended data:

People's Republic of China (PRC) State Food and Drug Administration (CFDA) is the directly affiliated institution responsible for the comprehensive supervision and management of drugs, medical devices, cosmetics, health foods and catering foods in the State Council, and is responsible for drafting the draft regulations on the supervision and management of food safety (including food additives and health foods, the same below), drugs (including traditional Chinese medicines and ethnic medicines, the same below), medical devices and cosmetics.

Formulate measures for the implementation of food administrative licensing and supervise its implementation, organize the formulation and publication of national pharmacopoeia and other standards and classification management systems for drugs and medical devices and supervise their implementation, formulate and organize the implementation of supervision, management and inspection systems for food, drugs, medical devices and cosmetics, and organize the investigation and punishment of major illegal acts.