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Lumason Approval History

FDA Approved: Yes (First approved October 10, 2014)
Brand name: Lumason
Generic name: sulfur hexafluoride lipid microsphere
Dosage form: Injectable Suspension
Company: Bracco Diagnostics Inc.
Treatment for: Diagnosis and Investigation

Lumason (sulfur hexafluoride lipid microsphere) is a contrast agent used for ultrasound imaging.

Development History and FDA Approval Process for Lumason

DateArticle
Oct 10, 2014Approval FDA Approves Lumason Ultrasound Imaging Agent

Further information

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