The U.S. Food and Drug Administration (U.S. FDA) has issued seven observations to Dr. Reddy’s Laboratories after an inspection of the generic drugmaker’s formulations manufacturing facility in ...

Three types of Power Stick deodorant, sold by both Walmart and Amazon, have been pulled from the shelves after it failed to ...

As the United States moves beyond the first months of the second Trump Administration, artificial intelligence has emerged as ...

Jalux Americas Inc. has issued a voluntary recall for multiple units of its cookies due to the undeclared presence of ...

The US Food and Drug Administration aims to revoke 52 standards of identity (SOI) across a swath of food categories, claiming the regulations are “obsolete and unnecessary.” Under the proposal, ...

The latest inspection comes 2 1/2 years after the agency allowed Sun Pharma to keep shipping some drugs to Americans even ...

FNP-223, previously known as ASN90, is a reversible and substrate-competitive O-GlcNAcase enzyme inhibitor. The oral investigational drug is expected to rapidly increase O-GlcNAcylated tau proteins, ...

A group of two Republicans and two Democrats in Congress want the federal government to do a deep dive into the human health ...

Federal health agencies including the NIH, FDA, and CDC laid off over 10,000 employees following a Supreme Court ruling.

More than 67,000 cases of Power Stick roll-on deodorant products have been recalled. They were sold at Target, Walmart, ...

The FDA has accepted for review the sBLA to expand the indication of Arexvy (RSV vaccine, adjuvanted) to adults aged 18 to 49 years who are at increased risk.

In a surprise, a FDA advisory panel voted that risks tied to a GSK blood cancer drug called Blenrep outweighed the benefits ...