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Entreprise · 11/03/20241 min de lecture

Revocation of Emergency Use of a Drug Product During the COVID-19 Pandemic; Availability

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Résumé

The Food and Drug Administration (FDA) is announcing the revocation of the Emergency Use Authorization (EUA) (the Authorization) issued to Eli Lilly and Co. (Lilly), for bamlanivimab and etesevimab administered together. FDA revoked the Authorization on December 14, 2023, under the Federal Food, Drug, and Cosmetic Act (FD&C Act). The revocation, which includes an explanation of the reasons for the revocation, is reprinted in this document.

Langue originale de la source: Federal Register — Food and Drug AdministrationOuvrir le communiqué original →

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