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For Use under Emergency Authorization EUA.

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Inset white boxes shown to identify areas of interest, with white arrows indicating blood vessels at post-surgery day 8 B and post-surgery day 20 D.

REGEN-COV is not authorized for pre-exposure prophylaxis for prevention of COVID-19.

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Table 5: Preparation of 600 mg of Casirivimab and 600 mg of Imdevimab for Subcutaneous Injections Prepare 600 mg of Casirivimab and 600 mg of Imdevimab Preparation of 4 Syringes Using Casirivimab and Imdevimab Co-formulated Vial Withdraw 2.

Kit 8:06 Did you satisfy my checklist? 5 mL of solution contains 300 mg of casirivimab, L-histidine 1.

The FDA has authorized the emergency use of REGEN-COV for the treatment of COVID-19 and the post-exposure prevention of COVID-19 under an Emergency Use Authorization EUA.

Imdevimab, a human IgG1 mAb, is a covalent heterotetramer consisting of 2 heavy chains and 2 light chains produced by recombinant DNA technology in Chinese hamster ovary CHO cell suspension culture and has an approximate molecular weight of 144.

Remove the casirivimab and imdevimab vials from refrigerated storage and allow to equilibrate to room temperature for approximately 20 minutes before preparation.