The FDA has announced that popular weight loss medication tirzepatide is no longer in shortage, potentially removing cheaper versions of the drug from the market by early 2025. Tirzepatide is the ...

Although the eggs were initially recalled just five days after distribution on November 27, the FDA reclassified the recall to Class 1 – the agency’s highest alert level – on Friday.

Nuvation Bio (NUVB) announced that the U.S. FDA has accepted the company’s NDA for taletrectinib, an investigational next-generation ROS1 tyrosine kinase inhibitor TKI , for the treatment of ...

FDA Proposes New Testing Rules to Ensure Cosmetics Are Asbestos-Free WASHINGTON (AP) — Cosmetic companies would have to take extra steps to ensure that any products containing talc are free of ...

The company states: “AVITA Medical (RCEL) announced that the FDA has approved its premarket approval, PMA, supplement for RECELL GO mini. As a line extension of the RECELL GO system, the RECELL ...

After hours: December 27 at 4:08:11 PM EST Loading Chart for ICON ...

THURSDAY, Dec. 26, (2024 HealthDay News) -- The U.S. Food and Drug Administration (FDA) announced on Monday the approval of the first generic version of a daily injectable GLP-1 medicine for ...

It’s a win for skeptical academics, including researchers at the University of Florida who petitioned the FDA to revisit the drug’s use in 2007 and again in 2015. For consumers it will likely ...

Tea made from Camellia sinensis is now eligible for the "healthy" designation. The North Eastern Tea Association (NETA) and the Indian Tea Association (ITA) have welcomed the U.S. Food and Drug ...

An icon in the shape of a lightning bolt. Impact Link Elon Musk's xAI has completed its Series C funding round, raising a total of $6 billion, it revealed in a Monday blog post. Musk's artificial ...

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