Food and Drug Administration

E13297

The Food and Drug Administration is a U.S. federal agency responsible for protecting public health by regulating food, drugs, medical devices, and other consumer products.

All labels observed (12)

How this entity was disambiguated

Statements (51)

Predicate Object
instanceOf federal agency
government organization
regulatory agency
abbreviation Food and Drug Administration self-linksurface differs
surface form: FDA
country United States of America
surface form: United States
employerOf commissioner of Food and Drugs
formed 1906
hasDivision Center for Biologics Evaluation and Research
Center for Devices and Radiological Health
Center for Drug Evaluation and Research
Center for Food Safety and Applied Nutrition
Center for Tobacco Products
Center for Veterinary Medicine
National Center for Toxicological Research
Office of Regulatory Affairs
headquartersCountry United States of America
surface form: United States
headquartersLocation Silver Spring, Maryland
jurisdiction United States government
surface form: federal government of the United States
legalBasis Federal Food, Drug, and Cosmetic Act
surface form: Federal Food, Drug, and Cosmetic Act of 1938

Pure Food and Drug Act of 1906
locatedIn Maryland
mission ensure safety and effectiveness of medical devices
ensure safety and security of the U.S. food supply
ensure safety of cosmetics and radiation-emitting products
ensure safety, efficacy, and security of human and veterinary drugs
protect public health
regulate tobacco products
parentAgency United States Department of Health and Human Services
performsFunction enforcement of labeling requirements
inspection of manufacturing facilities
issuance of recalls and safety alerts
post-market safety surveillance
pre-market approval of drugs
pre-market approval of medical devices
review of clinical trial data
setting food standards
regulates biologics
blood and blood products
cellular therapies
cosmetics
dietary supplements
food products
gene therapies
medical devices
over-the-counter drugs
prescription drugs
radiation-emitting electronic products
tobacco products
vaccines
veterinary products
website Food and Drug Administration self-linksurface differs
surface form: https://www.fda.gov

How these facts were elicited

Referenced by (217)

Full triples — surface form annotated when it differs from this entity's canonical label.

Zepbound regulatoryAgency Food and Drug Administration
this entity surface form: U.S. Food and Drug Administration
Cymbalta isApprovedBy Food and Drug Administration
this entity surface form: U.S. Food and Drug Administration
Alimta hasApprovalAgency Food and Drug Administration
this entity surface form: U.S. Food and Drug Administration
Taltz isApprovedBy Food and Drug Administration
this entity surface form: U.S. Food and Drug Administration
Emgality approvalBy Food and Drug Administration
this entity surface form: U.S. Food and Drug Administration
Loxo Oncology (acquired) regulatoryAgencyApproval Food and Drug Administration
subject surface form: Loxo Oncology
this entity surface form: U.S. Food and Drug Administration
Myriad Genetics regulatoryBody Food and Drug Administration
this entity surface form: U.S. Food and Drug Administration
onasemnogene abeparvovec approvedBy Food and Drug Administration
this entity surface form: U.S. Food and Drug Administration
risdiplam approvedBy Food and Drug Administration
this entity surface form: U.S. Food and Drug Administration
riluzole wasApprovedBy Food and Drug Administration
subject surface form: Riluzole
this entity surface form: U.S. Food and Drug Administration
edaravone approvedBy Food and Drug Administration
subject surface form: Edaravone
this entity surface form: U.S. Food and Drug Administration
edaravone approvedBy Food and Drug Administration
subject surface form: Edaravone
this entity surface form: FDA
Tegsedi approvedBy Food and Drug Administration
this entity surface form: U.S. Food and Drug Administration
Mounjaro approvedBy Food and Drug Administration
this entity surface form: U.S. Food and Drug Administration
Prozac isApprovedBy Food and Drug Administration
this entity surface form: U.S. Food and Drug Administration
Tareyton regulatedBy Food and Drug Administration
this entity surface form: U.S. Food and Drug Administration
Title 21 primaryRegulatoryAgency Food and Drug Administration
subject surface form: Title 21 of the Code of Federal Regulations
this entity surface form: U.S. Food and Drug Administration
Salem regulationSubject Food and Drug Administration
this entity surface form: U.S. Food and Drug Administration
DEKA Arm System regulatoryApproval Food and Drug Administration
this entity surface form: U.S. Food and Drug Administration
fampridine approvedBy Food and Drug Administration
this entity surface form: U.S. Food and Drug Administration
FDC Act enforcedBy Food and Drug Administration
Kefauver–Harris Drug Amendments of 1962 administeredBy Food and Drug Administration
this entity surface form: U.S. Food and Drug Administration
Medical Device Amendments of 1976 regulatoryAgency Food and Drug Administration
Medical Device Amendments of 1976 relatedTo Food and Drug Administration
Orphan Drug Act of 1983 administeredBy Food and Drug Administration
this entity surface form: U.S. Food and Drug Administration
Drug Price Competition and Patent Term Restoration Act of 1984 administeredBy Food and Drug Administration
this entity surface form: U.S. Food and Drug Administration
Food Safety Modernization Act of 2011 primaryAgency Food and Drug Administration
this entity surface form: U.S. Food and Drug Administration
Family Smoking Prevention and Tobacco Control Act of 2009 grantsAuthorityTo Food and Drug Administration
this entity surface form: U.S. Food and Drug Administration
Family Smoking Prevention and Tobacco Control Act of 2009 establishesWithin Food and Drug Administration
this entity surface form: U.S. Food and Drug Administration
Virginia Slims regulatedBy Food and Drug Administration
this entity surface form: U.S. Food and Drug Administration
Altria Group regulator Food and Drug Administration
this entity surface form: U.S. Food and Drug Administration
Prescription Drug User Fee Act of 1992 appliesToJurisdiction Food and Drug Administration
this entity surface form: United States Food and Drug Administration
Prescription Drug User Fee Act of 1992 administeredBy Food and Drug Administration
this entity surface form: U.S. Food and Drug Administration
Food and Drug Administration Amendments Act of 2007 primaryAgencyAffected Food and Drug Administration
this entity surface form: U.S. Food and Drug Administration
Food and Drug Administration Amendments Act of 2007 expandsAuthorityOf Food and Drug Administration
this entity surface form: U.S. Food and Drug Administration
Kool isRegulatedBy Food and Drug Administration
this entity surface form: U.S. Food and Drug Administration
FDA v. Brown & Williamson Tobacco Corp. petitioner Food and Drug Administration
Children's Health Defense regulatoryAttentionFrom Food and Drug Administration
this entity surface form: U.S. Food and Drug Administration
21st Century Cures Act providesFundingTo Food and Drug Administration
21st Century Cures Act affectsAgency Food and Drug Administration
Wilhelm Reich worksDestroyedBy Food and Drug Administration
this entity surface form: U.S. Food and Drug Administration
OASH worksWith Food and Drug Administration
National Vaccine Program Office coordinatesWith Food and Drug Administration
Actemra approvedBy Food and Drug Administration
this entity surface form: U.S. Food and Drug Administration
Xeloda hasApprovalAgency Food and Drug Administration
this entity surface form: U.S. Food and Drug Administration
faricimab approvedBy Food and Drug Administration
this entity surface form: U.S. Food and Drug Administration