Sermorelin's FDA Journey: Approved, Discontinued, and Compounded Sermorelin acetate (Geref) was FDA-approved in 1997 for pediatric GHD 1 and in 1990 for diagnostic use.26 The manufacturer discontinued Geref in 2008 due to "manufacturing difficulties," not safety or efficacy concerns.12 In 2013, the FDA confirmed it wasn't withdrawn for safety/effectiveness, allowing for potential generic approvals.12 Currently, Sermorelin is primarily available as a compounded medication 3, which is permitted but not individually FDA-approved like mass-produced drugs.22 5.2
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For the UDE, no toxic effect was observed for 1, 10, and 100 M -EC-containing UDE
Refrigerate After Opening : While some sources suggest that refrigeration is not strictly necessary for unopened bottles, we recommend refrigerating liposomal glutathione once opened
