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March 2022 Wegovy shortage listed with FDA after contract manufacturer stops deliveries

doi: 10.1007/s11033-022-07757-8 85 NiknamMMalekiMHKhakshourniaSRasouliMVakiliOShafieeSM

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Section 503A permits compounding of drug products as customized therapies for identified individual patients whose medical needs cannot be met by commercially available drug products. 503B compounding , on the other hand, is performed at outsourcing facilities, which are subject to stricter FDA oversight, including cGMP requirements, a requirement to register with FDA, periodic FDA inspections and an obligation to submit adverse event reports and other product-specific information to FDA