
FDA Warns 30 Telehealth Firms Over Misleading GLP-1 Claims
The FDA issued 30 warning letters to telehealth companies for misleading marketing of compounded GLP-1 products, the second wave in a crackdown on direct-to-consumer pharmaceutical ads. The letters allege claims of sameness with FDA-approved products and branding that obscures sourcing. Compounded drugs are not FDA-approved and are not the same as generics, as the FDA does not review their safety or efficacy before marketing.













