The FDA also gave its nod to Bristol Myers Squibb’s Cobenfy (xanomeline and trospium chloride), the first new class of antischizophrenia drug to be approved in decades. Roughly one-third of last ...

3. In a separate act passed in 2024, California moved to ban six of the nine FDA-approved artificial food dyes in public school food and drinks by 2027. Worried one of your favorite foods will be ...

officials said. The FDA said 10 nicotine pouches made by Philip Morris International—including mint-, cinnamon- and coffee-flavored Zyn pouches, among other flavors—could remain on the market ...

The FDA says that food companies will have until Jan. 15, 2027 to stop using the dye. Drugmakers will have an extra year, until January 2028, to comply with the change. Red 3, also known as ...

Nicotine pouches are tobacco-free sachets filled with nicotine and ... it does not mean the products are “safe, nor are they ‘FDA approved.’” FDA, in its review of existing data and ...

3. In a separate act passed in 2024, California moved to ban six of the nine FDA-approved artificial food dyes in public school food and drinks by 2027. The bill did not include Red No.

Indianapolis: Eli Lilly and Company has announced that the U.S. Food and Drug Administration (FDA) has approved Omvoh (mirikizumab-mrkz) for the treatment of moderately to severely active Crohn's ...

The tentative approval for ANDA 218862 was posted to the Drugs@FDA site. Discover outperforming stocks and invest smarter with Top Smart Score Stocks Filter, analyze, and streamline your search ...

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President-elect Donald Trump and his health nominees have not commented on the measure, but a similar effort led by Trump's first FDA commissioner, Dr. Scott Gottlieb, was sidelined during his ...

of the Campaign for Tobacco-Free Kids, in a statement. The FDA pointed to government survey data showing fewer than 2 percent of American high school and middle school students used nicotine ...

However, health advocates hail it as transformative. The public is invited to comment on this proposal, with the FDA planning for the ruling to take effect two years post-approval.