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FDA slams Novo Nordisk for misleading Ozempic ad in second warning

Another blow for Novo Nordisk as regulators crack down on deceptive drug ads. Will this latest FDA warning reshape how Ozempic is marketed?

The image shows an old advertisement for Dr. Brooke's Oriental Pills, featuring text and a logo....
The image shows an old advertisement for Dr. Brooke's Oriental Pills, featuring text and a logo. The text is written in a bold font and the logo is a circular shape with a white background and a blue border.

FDA slams Novo Nordisk for misleading Ozempic ad in second warning

The U.S. Food and Drug Administration (FDA) has issued a formal warning to Novo Nordisk over a misleading advertisement for Ozempic. The agency claims the commercial made false statements about the diabetes drug's benefits and downplayed safety risks. This marks the second reprimand for the company in less than a month.

The FDA's warning targets the Ozempic commercial titled 'There's Only One Ozempic'. Regulators argue the ad falsely suggests the drug has more FDA-approved uses than competitors, implying universal benefits without proper evidence. They also criticise the placement of safety warnings, which appear only after the closing jingle and manufacturer's logo, making them easy to overlook.

This latest action follows a similar warning last month regarding Novo Nordisk stock and its weight-loss drug Wegovy. The FDA has given the company 15 business days to submit a formal response to the allegations.

The crackdown is part of a wider FDA campaign against deceptive drug advertising. Over the past year, from March 2025 to March 2026, the agency has sent warning letters to 47 companies, including major firms like PharmaCorp and Medix Labs. The push for stricter oversight comes after an executive order by then-U.S. President Donald Trump calling for tougher regulation of pharmaceutical marketing.

Novo Nordisk must now address the FDA's concerns within the given deadline. The outcome could impact how the company advertises Ozempic and other drugs in the future. The case also highlights the agency's ongoing efforts to enforce transparency in pharmaceutical promotions.

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