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Category 2 is where compounds go when the FDA has determined they cannot be used in compounding typically because the agency has identified safety signals, insufficient data, or both
A Randomized Controlled Trial of the GLP-1 Receptor Agonist Dulaglutide in Primary Polydipsia. The Journal of Clinical Investigation
10.1111/bcpt.13306 96 YuzefovychL
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Both options contain the same active ingredient, yet they differ significantly in FDA approval status, manufacturing standards, cost, and potential risks
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