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Emergent BioSolutions Receives U.S. FDA Approval for Drug Product Manufacturing of raxibacumab at its Winnipeg, Canada Site

GAITHERSBURG, Md., Dec. 12, 2025 (GLOBE NEWSWIRE) -- Emergent BioSolutions (NYSE: EBS) today announced that the U.S. Food and Drug Administration (FDA) has approved its supplemental Biologics License Application (sBLA) for its Winnipeg, Canada facility to be added as the drug product manufacturing and testing site for raxibacumab, a monoclonal antibody for the treatment and prophylaxis of inhalational anthrax. “We are pleased with the U.S. FDA approval of our sBLA for raxibacumab manufacturing a

articleEmergent Biosolutions Inc.December 12, 20254/company/emergent-biosolutions-inc/news/emergent-biosolutions-receives-u-fda-133000086
Emergent BioSolutions Receives U.S. FDA Approval for Drug Product Manufacturing of raxibacumab at its Winnipeg, Canada Site

About this update from Emergent Biosolutions Inc.

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More updates from Emergent Biosolutions Inc.

Emergent BioSolutionsinhalational anthraxWinnipeg, Canadaraxibacumabtransformation strategyFood and Drug Administrationmanufacturing