Today, Novo Nordisk announced the submission of a sNDA to the U.S. Food and Drug Administration (FDA) for a higher dose of ...

Poherdy can be dispensed as a substitute for Perjeta without requiring a prescription change from a health care provider.

WASHINGTON (AP) — The head of the Food and Drug Administration’s drug center abruptly resigned Sunday after federal officials began reviewing “serious concerns about his personal conduct,” according ...

Dr. George Tidmarsh steps down after an online post criticizing a Canadian drug sparked a lawsuit alleging false claims and bribery. Trump admin weighs major change to Social Security disability ...

New York, Nov. 03, 2025 (GLOBE NEWSWIRE) -- New York, Monday, November 3, 2025 – The Muscular Dystrophy Association (MDA) marks another milestone today in our legacy of progress with the FDA approval ...

WASHINGTON (AP) - The Food and Drug Administration on Friday moved to limit the use of fluoride supplements used to strengthen children’s teeth, the latest action by Health Secretary Robert F. Kennedy ...

The FDA has added two more brands of ground cinnamon to its sweeping advisory about high levels of lead. Secret Service finds 17 'skimming' devices in tour of San Antonio businesses Unearthed records ...

The U.S. Food and Drug Administration plans to expedite approvals for nine experimental drugs The move includes treatments for cancer and fertility Approvals could now happen in as little as one to ...

Denali Therapeutics got an extension from the Food and Drug Administration for the review of its treatment for the genetic disorder Hunter syndrome. The target date for the license application review ...

- Updated indication allows the use of RINVOQ® (upadacitinib) prior to the use of tumor necrosis factor (TNF) blocking agents in patients for whom use of these treatments is clinically inadvisable and ...