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

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...

Food and Drug Administration may refer to: China Food and Drug Administration (NMPA) Food and Drug Administration, a government agency in the United States...

The National Agency for Food and Drug Administration and Control (NAFDAC) is a Nigerian federal agency under the Federal Ministry of Health that is responsible...

Numerous governmental and non-governmental organizations have criticized the U. S. Food and Drug Administration for alleged excessive and/or insufficient regulation...

The Food and Drug Administration is a federal agency of the United States, formed in 1930. Up until the 20th century, there were few federal laws regulating...

United States Congress, and led to the creation of the Food and Drug Administration (FDA). Its main purpose was to ban foreign and interstate traffic in...

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...

Food and Drug Administration is a ministry of the Government of Maharashtra. The ministry is responsible for consumer protection and regulating food and...

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

The Department of Food and Drug Administration (Burmese: အစားအသောက်နှင့် ဆေးဝါးကွပ်ကဲရေး ဦးစီးဌာန; abbreviated FDA) is Burma's food safety regulatory...

The Food and Drug Administration (FDA; Chinese: 食品藥物管理署) is an agency of the Ministry of Health and Welfare of Taiwan, which is responsible for the safety...

drug. A generic drug must contain the same active ingredients as the original brand-name formulation. The U.S. Food and Drug Administration (FDA) requires...

Food and Drug Administration, Maharashtra State, is Maharashtra's primary instrument of consumer protection. It is a law enforcement agency. In 1970, the...

The Food and Drug Administration Safety and Innovation Act of 2012 (FDASIA) is a piece of American regulatory legislation signed into law on July 9, 2012...

The Ministry of Food and Drug Safety (MFDS; Korean: 식품의약품안전처), formerly known as the Korea Food & Drug Administration (KFDA; 식품의약품안전청), is a government...

State Administration for Market Regulation. The agency had multiple former names, including China Food and Drug Administration and State Food and Drug Administration...

The United States Food and Drug Administration Modernization Acts (FDAMA) are amendments to the Federal Food, Drug, and Cosmetic Act, which regulated...

September 2022, in Canada in November 2022, and in Australia in December 2022. The US Food and Drug Administration (FDA) considers it a first-in-class medication...

the United States Food and Drug Administration that regulates food, dietary supplements, and cosmetics, The Food and Drug Administration (United States)...

ISBN 978-0-86196-607-3. Retrieved 29 June 2024. "New Drug Application (NDA) 008943". Drugs@FDA. U.S. Food and Drug Administration (FDA). Archived from the original on...

a significantly elevated risk of acute pancreatitis. The US Food and Drug Administration prescription label for semaglutide contains a boxed warning for...

semaglutide, and tirzepatide are approved by the US Food and Drug Administration (FDA) for weight management in combination with reduced-calorie diet and increased...

Center for Food Safety and Applied Nutrition, Inspections, Compliance, Enforcement, and Criminal Investigations, US Food and Drug Administration. Retrieved...

Prescription Drug Marketing Act (PDMA). The Food and Drug Administration (FDA) is charged with implementing the law. As a general rule, over-the-counter drugs (OTC)...

development and drug sales. In the U.S., the Elixir Sulfanilamide disaster led to the establishment of the Food and Drug Administration, and the 1938 Federal...

manufacture and sale of OTC substances are regulated by the Food and Drug Administration. The FDA requires that all "new drugs" obtain a New Drug Application...

S. Food and Drug Administration. 31 January 2018. Retrieved 18 April 2024. "FDA - Italy, MOU Regarding Safety Evaluation Data". U.S. Food and Drug Administration...

the label must bear a disclaimer that the Food and Drug Administration (FDA) "has not evaluated the claim" and that the dietary supplement product is not...

Adult and Pediatric Patients with Beta-thalassemia Who Require Regular Blood Transfusions" (Press release). U.S. Food and Drug Administration (FDA)....