NDC 0270-7097 – LumaSon

Sulfur Hexafluoride 60.7 mg/mg; Distearoylphosphatidylcholine, Dl- .19 mg/mg; Sodium 1,2-dipalmitoyl-sn-glycero-3-phospho-(1'-rac-glycerol) .19 mg/mg · Injection, Powder, Lyophilized, For Suspension · Intravenous, Intravesical

Human Prescription Drug

Product NDC0270-7097

Product details

Brand name
LumaSon
Generic name
Sulfur Hexafluoride
Labeler
BRACCO DIAGNOSTICS INC
Dosage form
Injection, Powder, Lyophilized, For Suspension
Route
Intravenous, Intravesical
Marketing category
NDA · NDA203684
Marketed since
April 1, 2021
Listing expires
December 31, 2026
Pharmacologic class
Contrast Agent for Ultrasound Imaging

Active ingredients

Uses, dosage, side effects and warnings for LumaSon →

Package NDC codes (2)

Package NDCDescriptionSince
0270-7097-0720 VIAL in 1 BOX (0270-7097-07) / 25 mg in 1 VIALApr 1, 2021
0270-7097-0820 VIAL in 1 BOX (0270-7097-08) / 25 mg in 1 VIALApr 1, 2021

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