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  2. FDA warns companies over unapproved weight loss drug sales - AOL

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    The Food and Drug Administration (FDA) announced in a statement Tuesday that it has sent warning letters to companies selling unapproved weight loss drugs. The letter went to Xcel Peptides ...

  3. US FDA warns online vendors selling unapproved weight-loss drugs

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    The agency also sent a warning letter to Veronvy, which offers unapproved and misbranded oral GLP-1 products, including one that claims to be approved by the FDA. US FDA warns online vendors ...

  4. FDA warns against unapproved 'fat-dissolving' spa treatments

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    However, the FDA on Wednesday noted the presence of unapproved fat-dissolving injections popping up at clinics and med spas across the U.S., including those sold online under brand names like ...

  5. US FDA warns online vendors to stop selling unapproved weight ...

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    The U.S. Food and Drug Administration (FDA) on Tuesday published letters warning two online vendors to stop selling unapproved versions of semaglutide and tirzepatide, the active ingredients in ...

  6. FDA warns online vendors selling misbranded weight-loss ... - AOL

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    Novo and its biggest rival in the obesity drug market, Eli Lilly, sued several medical spas, weight-loss clinics and compounding pharmacies last year to stop them from selling products purporting ...

  7. US FDA says Lilly’s weight-loss drug shortage is resolved

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    The U.S. Food and Drug Administration said on Thursday there was no longer a shortage of Eli Lilly’s (LLY.N) blockbuster weight loss and diabetes drugs following a re-evaluation of their supply ...

  8. FDA warns against unapproved ‘fat-dissolving’ spa treatments

    www.aol.com/news/fda-warns-against-unapproved...

    The FDA issued a warning about the dangers of using unauthorized versions of fat-dissolving injections, saying it has received reports of severe side effects. FDA warns against unapproved ‘fat ...

  9. FDA shakes up weight loss market as Mounjaro shortage ends - AOL

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    The FDA made it clear in its announcement that a “compounded drug may not be identical or nearly identical to an FDA-approved drug unless the approved drug is on FDA’s drug shortage list.”

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