Semaglutide
Semaglutide has FDA-approved prescription products (OZEMPIC (NDA209637), OZEMPIC / RYBELSUS (NDA213051), RYBELSUS (NDA213182), WEGOVY (NDA218316), WEGOVY / WEGOVY FLEXTOUCH / WEGOVY HD (NDA215256)). FDA's drug shortage database lists 3 Semaglutide entries (To Be Discontinued) as of 2026-07-25; that describes supply of an approved product, not whether compounding is lawful. Semaglutide is not on FDA's 503B Bulks List for outsourcing facilities (list checked 2026-07-25). 50 registered ClinicalTrials.gov studies cite Semaglutide (25 completed, 12 recruiting, 6 not yet recruiting, 3 active not recruiting, 2 enrolling by invitation, 2 unknown); registration is not evidence of approval, efficacy, or safety. CompoundedGuide is verifying compounding status, safety signals, and current evidence. This is not medical advice.