Will an FDA crackdown curb access to cheaper GLP-1 weight-loss drugs?

The Food and Drug Administration has warned a major compounding pharmacy that it violated federal law by making copies of blockbuster weight-loss drug s in "inordinate amounts."

The letter to Empower Pharmacy marks the first time the FDA has waded into a fierce debate about when a pharmacy's legitimate work of customizing a medication crosses the line into mass-copying of patented FDA-approved drugs.

The FDA's warning, dated Sept. 18 but posted online Tuesday, gives Houston-based Empower an opportunity to comply with the FDA's requirements. In a statement, Empower said it has "already remediated many of the issues outlined in the Warning Letter," adding that it will "continue to work cooperatively with the agency to ensure patient access to quality compounded drug products."

Empower openly advertises two of the most popular medications on its website, which are available to healthcare providers and not directly to consumers.

Compounding pharmacies have traditionally custom-tailored medications for individual patients, such as making a liquid solution for someone who can't swallow a pill. Regulators inspect their facilities but don't review the medications they make. Because of this, the FDA says it can't offer the same safety assurances as drugs that go through its rigorous approval process.

With the frenzy ignited by GLP-1 weight-loss drugs , compounding pharmacies have found a new opportunity. FDA regulations allow them to make copies of brand-name drugs when the agency declares a shortage . So when the FDA determined that Novo Nordisk and Eli Lilly couldn't keep up with demand for their appetite-suppressing drugs in 2022, many compounders jumped at the chance to make their own versions, drawing millions of patients with much cheaper prices.

This is where things get contentious. The FDA declared an end to the shortage in 2025. Federally licensed compounding pharmacies — which are permitted to make larger quantities of medications and have to comply with more exacting standards — have largely stopped making copies of Eli Lilly's tirzepatide (marketed as Zepbound and Mounjaro) and Novo's semaglutide (sold as Wegovy and Ozempic). But smaller, state-licensed pharmacies have continued to make versions of these drugs, citing an FDA policy that allows them to tweak an approved drug — altering the dosage, or combining it with a vitamin — when a licensed medical professional says the change will make a "significant difference" for an individual patient.

Eli Lilly and Novo have loudly objected to this practice in public statements and lawsuits.