Drug Approvals and Databases | FDA
Drug Approvals and Databases | FDA
Drugs | FDA - U.S. Food and Drug Administration
Explore the FDA's Center for Drug Evaluation and Research, ensuring access to safe and effective drugs in the United States.
Drugs@FDA Data Files | FDA - U.S. Food and Drug Administration
Drugs@FDA Downloadable Data File in ZIP format, Data Definitions, and Entity Relationship Diagram (ERD)
Drugs@FDA - Food and Drug Administration
Drugs@FDA allows you to search for official information about FDA approved innovator (brand name) and generic drugs and therapeutic biological products.
U.S. Food and Drug Administration
2024年12月23日 · The FDA is responsible for protecting the public health by ensuring the safety, efficacy, and security of human and veterinary drugs, biological products, and medical devices; and by ensuring the ...
Find Information about a Drug | FDA - U.S. Food and Drug Administration
2022年8月9日 · Search FDA Approved Drugs on Drugs@FDA. Explore the database to find drug labels (package inserts), generics, patient information, FDA review and approval history
FDA Label Search
Drugs @ FDA, where information about FDA-approved human brand name and generic drugs as well as therapeutic biological products is available. Biologics Products and Establishments , where...
Drugs@FDA Database - Catalog
2023年7月26日 · Information about FDA-approved brand name and generic prescription and over-the-counter human drugs and biological therapeutic products. Drugs@FDA includes most of the drug products approved since 1939.
DailyMed
2021年9月15日 · The National Library of Medicine (NLM)’s DailyMed searchable database provides the most recent labeling submitted to the Food and Drug Administration (FDA) by companies and currently in use (i.e., "in use" labeling). DailyMed contains labeling for prescription and nonprescription drugs for human and animal use, and for additional products ...
2018年5月8日 · The FFDCA allows FDA to require a manufacturer to conduct postapproval studies of drugs. The law specifies when FDA must attach that requirement to the NDA approval and when FDA may issue the requirement after a drug is on the market. To manage exceptional risks of drugs, FDA