Dec 23 (Reuters) - US FDA:
* US FDA: REVOKED EMERGENCY USE AUTHORIZATION FOR LILLY'S BEBTELOVIMAB AS OF DEC 13 - WEBSITE
* US FDA: REVOKED EMERGENCY USE AUTHORIZATION FOR ASTRAZENECA'S EVUSHELD AS OF DEC 13 - WEBSITE
* US FDA: REVOKED EMERGENCY USE AUTHORIZATION FOR REGENERON'S REGEN-COV AS OF DEC 13 - WEBSITE
* US FDA: REVOKED EMERGENCY USE AUTHORIZATION FOR GSK AND VIR BIOTECHNOLOGY'S SOTROVIMAB AS OF DEC 13 - WEBSITE
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