retatrutide clinical trial safety profile trials The FDA has issued warning letters to multiple companies marketing compounded retatrutide clinical trial safety Retatrutide

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Reconstituted vials must be labelled with the date and time of preparation, concentration, and beyond-use date in accordance with the protocol and local aseptic policy

Product Specifications Active Compound: Retatrutide peptide Strength: 30mg per vial Form: Lyophilized powder Reconstitution Required: Yes, according to a validated laboratory protocol Manufacturer, as listed: Novera Compounds Country of Origin, as listed: United States Brand: Novera Intended Use: Laboratory and in vitro research only Package Content: 1 x 30mg vial Weight: 7 grams Dimensions: Width: 20mm | Height: 40mm | Length: 20mm Human-Use Status: Not approved for human use, clinical application, injection, or consumption Researchers should verify the product label, certificate of analysis, batch identity, purity method, storage requirements, safety data sheet, and manufacturer information before use

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