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The FDA distinguishes the categories explicitly: a generic is approved under section 505(j) and must establish therapeutic equivalence to a brand-name drug, while a compounded drug is not FDA-approved and the agency does not verify its safety, effectiveness or quality before marketing

10.4238/gmr.15038330 Genet

Diabetologia (2024): Network meta-analysis of GLP-1 and dual agonist medications * Illustrative images on this page are models, not actual patients

Rest assured that every procedure uses drugs and techniques approved by the FDA and supported by extensive research and clinical trials