The FDA has approved GRAFAPEX™ and fludarabine as a preparative regimen in acute myeloid leukemia or myelodysplastic syndrome prior to alloHSCT.

STATEN ISLAND, N.Y. — A popular brand of cookies has been recalled across the United States for containing “life-threatening' allergens, according to the Food and Drug Administration (FDA).

The FDA wants food and beverage manufacturers to display nutrition labels on the front of most of their packages in an effort to help Americans make healthier choices.

After a delayed approval, treosulfan’s manufacturer is hopeful the alkylating agent will become the new gold standard in the United States.

Red dye No. 3 has been permissible for use in food despite the Delaney Clause of the FDA’s Federal Food, Drug, and Cosmetic Act. The clause, in part, “prohibits the FDA from approving a color additive that is ingested if it causes cancer in animals or humans when ingested,” according to the agency .

T he U.S. Food and Drug Administration (FDA) banned the use of Red Dye No.3 in foods and has given drug manufacturers until Jan. 18, 2028, and food manufacturers until Jan. 15, 20

The proposed "Nutrition info box" would show customers whether products have low, medium or high levels of saturated fat, sodium and added sugars.

The FDA is proposing a limit on the amount of nicotine in cigarettes and certain other combustible tobacco products to reduce their addictive properties.

The authors write "The Food, Drug and Cosmetic Law Section of the New York State Bar Association is delving into the changing face of health law and regulations as part of its Annual Meeting taking place Jan.

Drug companies in the U.S. are spending $4 billion a year on TV ads touting the drug benefits with rapid-fire list of possible side effects.

The Republican-led states of Idaho, Missouri and Kansas can proceed with a lawsuit seeking to restrict the availability of the abortion pill mifepristone in the United States, a federal judge in Texas ruled on Thursday.