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Drug compounding rules and FDA actions to monitor

FDA shapes compounding through its guidance, its risk alerts, its enforcement actions and its drug shortage list, which affects when compounded versions of a drug can be made. These are the pages where FDA, the Federal Register and the national pharmacy bodies post those changes.

For semaglutide and tirzepatide, the shortage list and FDA's statements on unapproved GLP-1 drugs are the pages to read.

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The pages in this topic

FDA's compounding actions, risk alerts and policies, the drug shortage list, its letters on drug marketing, the Federal Register's compounding and GLP-1 notices, and the national pharmacy bodies.

We last checked every page here on October 20, 2026.

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To hear only about what matters to you, add keywords such as “semaglutide”, “tirzepatide”, “GLP-1”, “503A”, “503B”, “outsourcing facility”, “bulk drug substance”.

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