Food and Drug Administration (FDA or US FDA) is a federal agency of the Department of Health and Human Services. The FDA is responsible for protecting...

FDA Consumer was a magazine published from 1967 through 2007 by the U.S. Food and Drug Administration (FDA). From 1967 to 1972 it was known as FDA Papers...

commissioner of food and drugs is the head of the Food and Drug Administration (FDA), an agency of the United States Department of Health and Human Services...

Look up FDA in Wiktionary, the free dictionary. FDA or Food and Drug Administration, is an agency responsible for the control and safety of food and drugs...

States Supreme Court case to challenge the U.S. Food and Drug Administration (FDA)'s approval of mifepristone, a drug frequently used in medical abortion procedures...

excessive and/or insufficient regulation. The U.S. Food and Drug Administration (FDA) is an agency of the United States Department of Health and Human Services...

S. Food and Drug Administration (FDA) to oversee the safety of food, drugs, medical devices, and cosmetics. The FDA's principal representative with members...

FDA v. Wages and White Lion Investments, L.L.C. is a pending United States Supreme Court case about the Food and Drug Administration's denial of approval...

The US Food and Drug Administration (FDA) considers it to be a first-in-class medication. It was approved by the FDA for weight loss in November 2023. In...

or after the 2008 FDA communication and prescribing information changes that first publicized the concern. In addition, the FDA's analysis summary of...

2019. He has been a frequent critic of the Food and Drug Administration (FDA), and was considered by Donald Trump to lead the agency during his first...

into her" ft. Kirko Bangz - Fame" (2015) "FDA Music: Overgrind". 24Hour HipHop. Retrieved 2015-08-13. "FDA Music feat. Kirko Bangz: 'All Into Her'". AllHipHop...

utmost importance. The FDA can require a pharmaceutical company to place a boxed warning. It is the strongest warning that the FDA requires, and signifies...

Administration's (FDA) New Drug Application (NDA) is the vehicle in the United States through which drug sponsors formally propose that the FDA approve a new...

February 2022. "FDA-sourced list of all drugs with black box warnings (Use Download Full Results and View Query links.)". nctr-crs.fda.gov. FDA. Retrieved...

the Food and Drug Administration (FDA) was given the ability to regulate tobacco products. Prior to 1996, the FDA played no role in the regulation of...

Administration (FDA) due to its genetic health tests; as of October 2015, DNA tests ordered in the US include a revised health component, per FDA approval....

a severe undesired side effect. The U.S. Food and Drug Administration (FDA) has indicated that "it does not appear that the risk [of rhabdomyolysis]...

FDA preemption is the legal theory in the United States that products licensed or otherwise approved for use by the Food and Drug Administration (FDA)...

FDA v. Brown & Williamson Tobacco Corp., 529 U.S. 120 (2000), is an important United States Supreme Court case in U.S. administrative law. It ruled that...

lacking placebo-controlled trials, means that few modern drugs have earned FDA approval as initial monotherapy. In contrast, Europe only requires equivalence...

Breastfeeding "FDA-sourced list of all drugs with black box warnings (Use Download Full Results and View Query links.)". nctr-crs.fda.gov. FDA. Retrieved...

9 July 2012 Food and Drug Administration Safety and Innovation Act. The FDA's "breakthrough therapy" designation is not intended to imply that a drug...

The Food and Drug Administration (FDA) of the Philippines, formerly the Bureau of Food and Drugs (BFAD /ˈbiːfæd/; 1982–2009), is a health regulatory agency...

Administration (FDA) is authorized to perform inspections under the Federal Food, Drug, and Cosmetic Act, Sec. 704 (21 USC §374) "Factory Inspection". Form FDA 483...

AbobotulinumtoxinA is the first and only FDA-approved botulinum toxin for the treatment of pediatric lower limb spasticity. In the US, the FDA approves the text of the...

An FDA citizen petition is a process provided by the United States Food and Drug Administration (FDA) for individuals and community organizations to make...

manufactured foods remains illegal under FDA regulation, as of 2024[update]. In the United States, the FDA has indicated only one brand of prescription...

publication produced by the United States Food and Drug Administration (FDA), as required by the Drug Price and Competition Act (Hatch-Waxman Act). The...

(NLEA), per the recommendations of the FDA. It was one of several controversial actions taken during the tenure of FDA Commissioner Dr. David Kessler. The...