The U.S. Food and Drug Administration says drug makers have recalled more than a half-million bottles of the blood pressure ...
Two new deaths and seven more illnesses have been reported in an expanding outbreak of listeria food poisoning tied to ...
More than 580,000 blood pressure capsules have been recalled over cancer concerns. Here's how hypertension affects the Ohio ...
The agency announced moves to cut regulatory obstacles for the makers of biosimilar drugs, which are akin to generics and may ...
Federal regulators are trying to make it easier to develop cheaper alternatives to powerful drugs that many Americans depend ...
WuXi AppTec, a global contract research, development, and manufacturing organization (CRDMO), recently hosted its 2025 ...
By Jonathan Stempel (Reuters) -The makers of Tylenol, Johnson & Johnson and Kenvue, were sued on Tuesday by Texas Attorney ...
Citing a ProPublica investigation, lawmakers are calling on the FDA to conduct more drug testing and to alert hospitals and ...
The Food and Drug Administration uses import alerts to enforce U.S. food safety regulations for food from foreign countries.
The US Food and Drug Administration will take steps to streamline the process to develop generic versions of complex biological drugs, the agency announced Wednesday. The changes are meant to ...
A month’s supply of Miebo requires $800 and a prescription in the U.S. In Europe, it’s over-the-counter and $20.
If approved, it would be the first major new drug treatment for Parkinson’s in half a century. Richard Mailman, a University ...