Hims & Hers Pulls Wegovy Pill Dupe After FDA Threats — Novo Nordisk Files Patent Lawsuit Anyway
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Hims & Hers Pulls Copycat Wegovy Pill After FDA Threats

The telehealth company bowed to pressure from the FDA and Novo Nordisk. What does that mean for the future of other compounded GLP-1s?
Hims & Hers Pulls Copycat Wegovy Pill After FDA Threats
Everyday Health

A fast-moving legal and regulatory battle over a copycat Wegovy pill prompted its maker, the telehealth company Hims & Hers, to pull the product from the market two days after its launch in early February.

The saga isn’t over, as the manufacturer of the original Wegovy pill, Novo Nordisk, has filed a lawsuit alleging copyright infringement.

On February 5, Hims & Hers announced plans to offer a compounded semaglutide pill for as little as $49 per month, positioning it as a lower-cost alternative to the brand-name Wegovy pill. The company claimed it contained the same active ingredient (semaglutide) found in Wegovy and Ozempic.

The announcement immediately drew skepticism from obesity specialists and regulators, who cautioned that compounded drugs are not approved by the U.S. Food and Drug Administration (FDA) and are not required to undergo large clinical trials to prove safety, effectiveness (including consistent absorption), and manufacturing quality.

FDA Threatens Legal Action on Compounded GLP-1s

One day after Hims & Hers launched their compounded semaglutide pill, federal officials responded. The FDA's commissioner, Martin A. Makary, MD, MPH, announced that the agency intended to take “decisive steps” to restrict non-FDA-approved compounded drugs that are mass-marketed as alternatives to approved GLP-1s.

“These actions are aimed to safeguard consumers from drugs for which the FDA cannot verify quality, safety, or efficacy,” Dr. Makary said in a statement.

The FDA also warned companies against marketing compounded GLP-1 products as “generic” versions of FDA-approved drugs or claiming they are clinically proven to deliver the same results.

Soon after, Mike Stuart, general counsel for tktktk, posted on X that the U.S. Department of Health and Human Services had referred Hims & Hers to the Department of Justice for investigation over potential violations of the Federal Food, Drug, and Cosmetic Act and other federal statutes, which Makary reposted.

Hims & Hers Action May Be a ‘Tipping Point’

On Saturday, February 7, Hims & Hers said it would stop offering the pill.

“Since launching the compounded semaglutide pill on our platform, we’ve had constructive conversations with stakeholders across the industry,” the company said in a statement posted to X. “As a result, we have decided to stop offering access to this treatment.”

The reversal was not sufficient for the maker of Wegovy. On Monday, February 9, Novo Nordisk filed a U.S. patent infringement lawsuit against Hims & Hers, covering both pill and injectable versions of semaglutide products. It’s the first time Novo Nordisk has filed a U.S. patent case against a compounder.

The Danish company is asking the court to permanently bar Hims from selling compounded drugs that it alleges infringe on its patents and is seeking monetary damages.

"There is now a growing chorus of parties that have said, ‘Enough is enough on the compounding situation in the United States,’” said Novo Nordisk’s general counsel, John Kuckelman, as reported by Reuters; he called the Hims & Hers pill launch a “tipping point.”

Tensions Rise Between Drug Accessibility and Safety

Hims & Hers frames the lawsuit as a “blatant attack” by Novo on “millions of Americans who rely on compounded medications for access to personalized care.”

"Once again, Big Pharma is weaponizing the U.S. judicial system to limit consumer choice," said a Hims spokesperson.

When the company first announced the compounded semaglutide pill, experts told Everyday Health that expanded access shouldn’t come at the expense of rigorous safety and efficacy testing.

“These products have not been tested in large, randomized clinical trials, may vary in strength or purity, and may not even contain the same active ingredient as FDA-approved semaglutide,” said Fatima Cody Stanford, MD, MPH, an obesity medicine specialist at Massachusetts General Hospital and Harvard Medical School, both in Boston.

“Obesity is a chronic disease that deserves evidence-based treatment. Lowering standards for safety and efficacy for people with obesity reinforces harmful inequities in care,” Dr. Stanford said. “Patients should not be asked to accept unproven therapies simply because effective, FDA-approved options are expensive or difficult to access.”

The Future of Compounded GLP-1s Is Uncertain

Under U.S. law, compounding pharmacies are allowed to create customized medications in certain circumstances, such as when a patient needs a dose or formulation that’s different from what is commercially available.

The initial rollout of new GLP-1 drugs was plagued by shortages, and compounding pharmacies like Hims & Hers stepped in to fill high demand.

Some compounded GLP-1s have remained on the market even as shortages eased, with compounders in a legal “gray zone” relying on provisions that allow for personalized formulations.

It’s unclear what the future holds for people who have relied on compounded GLP-1s. The FDA statement suggests that other companies offering unapproved versions of the weight loss drugs may be subject to legal action, including injunction and seizure of the drugs.

EDITORIAL SOURCES
Everyday Health follows strict sourcing guidelines to ensure the accuracy of its content, outlined in our editorial policy. We use only trustworthy sources, including peer-reviewed studies, board-certified medical experts, patients with lived experience, and information from top institutions.
Resources
  1. Jacobsen S et al. Novo Nordisk Sues Hims After $49 Weight-Loss Pill Sparks FDA Backlash. Reuters. February 9, 2026.
  2. More Options, More Support: New Compounded Semaglutide Pill from Hims & Hers. Hims & Hers Newsroom. February 5, 2026.
  3. FDA Intends to Take Action Against Non-FDA-Approved GLP-1 Drugs. U.S. Food and Drug Administration. February 6, 2026.
  4. Human Drug Compounding. U.S. Food and Drug Administration. February 2, 2026.

Emily Kay Votruba

Fact-Checker
Emily Kay Votruba has copy edited and fact-checked for national magazines, websites, and books since 1997, including Self, GQ, Gourmet, Golf Magazine, Outside, Cornell University Press, Penguin Random House, and Harper's Magazine. Her projects have included cookbooks (Padma Lakshmi's Tangy Tart Hot & Sweet), self-help and advice titles (Mika Brzezinski's Know Your Value: Women, Money, and Getting What You're Worth), memoirs (Larry King's My Remarkable Journey), and science (Now You See It: How the Brain Science of Attention Will Transform How We Live, Work, and Learn, by Cathy Davidson). She started freelancing for Everyday Health in 2016.
Becky Upham, MA

Becky Upham

Author

Becky Upham has worked throughout the health and wellness world for over 25 years. She's been a race director, a team recruiter for the Leukemia and Lymphoma Society, a salesperson for a major pharmaceutical company, a blogger for Moogfest, a communications manager for Mission Health, a fitness instructor, and a health coach.

Upham majored in English at the University of North Carolina and has a master's in English writing from Hollins University.

Upham enjoys teaching cycling classes, running, reading fiction, and making playlists.