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What the April 30 Notice Actually Says On April 30, 2026, the FDA published a Federal Register notice (Docket FDA-2018-N-3240, Federal Register document 2026-08552) proposing to exclude three GLP-1 receptor agonists from the 503B Bulks List the list of bulk drug substances for which FDA has determined there is a clinical need permitting outsourcing facility compounding from raw active pharmaceutical ingredient

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References MacDonald, H

However, these products often contain bioactive ingredients that can influence hormone activity, metabolism, or related systems, which means they arent appropriate for everyone