Hyderabad based Natco pharma and its associate Lupin Limited got yet another US FDA approval for manufacture of Bosentan ...
The legislation permanently reclassifies fentanyl as a Schedule I drug, meaning it has no accepted medical use and a high ...
A bipartisan group of lawmakers in the House passed the HALT Act on Thursday, a bill that seeks to permanently classify ...
Breadcrumbs sold for months throughout the United States contain an undeclared allergen and are being recalled for safety reasons, the Food and Drug Administration announced on its website on Jan.
Breadcrumbs sold for months throughout the United States contain an undeclared allergen and are being recalled for safety reasons, the Food and Drug Administration announced on its website on Jan. 28.
Marijuana laced with fentanyl, the zombie drug xylazine, and nitazenes were listed as the top concerns people will face in the evolving drug ecosystem, during a Thursday hearing before the House ...
Prominent health care organizations urge the Trump administration to restore important data sets on the Centers for Disease ...
Several executive orders recently signed by US President Donald Trump may have significant implications for the US Food and Drug Administration ...
Does it feel like you know a lot of people fighting the flu virus this winter? The Centers for Disease Control and Prevention ...
The U.S. Food and Drug Administration said it approved Vertex Pharmaceuticals’ Journavx for short-term pain that often follows surgery or injuries.
The recalled product was manufactured in Italy and exported into the United States by Importations Piu Che Dolci Inc. of Quebec, Canada. The FDA said it was notified about the outbreak on Jan. 21 ...