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Description

Researchers running multi-week protocols should plan their reconstitution volumes to match their dosing schedule reconstituting only what will be used within the stable window prevents waste from compound degradation

Minor differences in the appearance of the lyophilized peptide between production lots are normal and generally reflect variations in freeze-drying conditions rather than differences in peptide identity or analytical purity

Sermorelins FDA status Sermorelin was FDA-approved in 1997 as Geref, but its manufacturer (EMD Serono) voluntarily discontinued it and requested withdrawal of the new drug application in December 2008