NDC 0270-7097-08

LumaSon .19 mg/mg

SULFUR HEXAFLUORIDE · INJECTION, POWDER, LYOPHILIZED, FOR SUSPENSION

No Recall History

LumaSon is a injection, powder, lyophilized, for suspension containing sulfur hexafluoride at a strength of .19 mg/mg. Manufactured by BRACCO DIAGNOSTICS INC.

Key Facts

Brand Name: LumaSon
Generic Name: SULFUR HEXAFLUORIDE
NDC Code (Package): 0270-7097-08
NDC Code (Product): 0270-7097
Manufacturer: BRACCO DIAGNOSTICS INC
Strength: .19 mg/mg
Dosage Form: INJECTION, POWDER, LYOPHILIZED, FOR SUSPENSION
Route: INTRAVENOUS, INTRAVESICAL
Marketing Status
Application #: NDA203684
Drug Class: Contrast Agent for Ultrasound Imaging [EPC]
Marketing Start: 04/01/2021

Recall History

No Recall History

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