Henry Ford Hospital dermatologist Dr. Henry Lim says the government has issued stricter standards for using the term “broad spectrum.”
The Food and Drug Administration has approved another new treatment for the chronic liver disorder known as Hepatitis C.
Allegan-based Perrigo Co. (Nasdaq: PRGO) announced that it has received final approval from the United States Food and Drug Administration for its abbreviated new drug application for over-the-counter Ranitidine 150 (regular and cool mint), a generic version of Zantac 150.
Allegan-based Perrigo Co. has received final approval from the United States Food and Drug Administration for its abbreviated new drug application for over-the-counter Minoxidil Foam, a generic version of Men’s Rogaine Foam
Allegan-based Perrigo Co. announced that it had achieved “acceptable regulatory status” in a re-inspection of its Allegal manufacturing plant by the Detroit office of the United States Food and Drug Administration.
The Food and Drug Administration wants to know if there could be a link between the artificial food coloring and hyperactivity in children.
Terumo Cardiovascular Systems, an Ann Arbor-based subsidiary of Terumo Corporation of Tokyo, Japan, announced it has agreed to the terms of a consent decree with the U.S. Food & Drug Administration regarding quality system improvements at the company’s Ann Arbor plant.
If you are just settling in to enjoy your peanut butter sandwich, please check the label to make sure you are not affected by the latest recall.
Lansing-based Neogen Corp. (Nasdaq: NEOG) announced that its rapid tests for salmonella meet the guidance for salmonella in animal feed currently being considered by the United States Food and Drug Administration.
Lansing-based Neogen Corp. (Nasdaq: NEOG) Wednesday announced that its rapid test for Salmonella enteritidis has been determined by the United States Food and Drug Administration to be equivalent to the FDA’s traditional testing method in accuracy, precision, and sensitivity for detecting SE.