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According to an agency press release issued Tuesday, the enforcement action centers on telehealth firms that marketed compounded versions of semaglutide, tirzepatide and liraglutide products, in ways that suggested equivalence with FDA-approved therapies such as Wegovy, Ozempic, Mounjaro and Zepbound

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Retatrutide is an investigational compound in late-stage clinical trials and has not been FDA-approved for any indication as of the publication date of this article