NDC 68155-099

LumaSon

Sulfur Hexafluoride

LumaSon is a Kit in the Human Prescription Drug category. It is labeled and distributed by Bracco Suisse Sa. The primary component is .

• Product ID: 68155-099_63be8d29-a289-59bc-fb3f-5ae8c9672bef
• NDC: 68155-099
• Product Type: Human Prescription Drug
• Proprietary Name: LumaSon
• Generic Name: Sulfur Hexafluoride
• Dosage Form: Kit
• Marketing Start Date: 2015-01-15
• Marketing Category: NDA / NDA
• Application Number: NDA203684
• Labeler Name: Bracco Suisse SA
• Active Ingredient Strength: 0
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 68155-099-16

5 KIT in 1 BOX (68155-099-16) > 1 KIT in 1 KIT * 25 mg in 1 VIAL * 5 mL in 1 SYRINGE

• Marketing Start Date: 2015-01-15
• NDC Exclude Flag: N
• Sample Package?: N

Drug Details

OpenFDA Data

• SPL SET ID: 5f81c772-fb18-08ad-7a0b-1a7f47329bc9
• Manufacturer:
  • Bracco Suisse SA

NDC Crossover Matching brand name "LumaSon" or generic name "Sulfur Hexafluoride"

NDC	Brand Name	Generic Name
0270-7097	Lumason	SULFUR HEXAFLUORIDE
0270-7099	LumaSon	SULFUR HEXAFLUORIDE
68155-099	LumaSon	SULFUR HEXAFLUORIDE