FDA
FDA (noun) means the United States Food and Drug Administration, the federal agency responsible for approving and regulating medicines, medical devices, food, cosmetics and tobacco products. Example: “The drug received FDA approval after two large trials.”
How to use FDA
Learner’s notesIn plain EnglishThe FDA is the US government body that decides which medicines and foods are safe to sell.
Takes the definite article: the FDA. FDA-approved and FDA-cleared are hyphenated before a noun and mean different things in law.
The FDA is American. The UK equivalent is the MHRA and the EU's is the EMA, so FDA approval means nothing outside the US on its own.
Trace the full origin ↓Fill the gap
Can you complete this real example?
The drug received _____ approval after two large trials.
Etymology
An initialism of Food and Drug Administration.
Synonyms
View more →Frequently asked questions
What is the difference between FDA-approved and FDA-cleared?
Approved means the FDA reviewed evidence that the product is safe and effective for its stated use — the standard for new drugs and high-risk devices. Cleared is a lighter route for devices, meaning the maker showed it is substantially equivalent to something already on the market.
What is the difference between the FDA and the USDA?
The FDA regulates most foods, all human and animal drugs, medical devices, cosmetics and tobacco. The USDA regulates meat, poultry and processed egg products, along with farming policy more broadly.
Does the FDA approve dietary supplements?
No. Supplements are sold without pre-market approval; the FDA can only act after a product reaches the market and proves unsafe or falsely labelled. A supplement bottle claiming to be FDA-approved is misrepresenting the rules.
What is the meaning of FDA?
"FDA" (noun) means the United States Food and Drug Administration, the federal agency responsible for approving and regulating medicines, medical devices, food, cosmetics and tobacco products.