0270-7097 : Lumason Intravenous; Intravesical Injection, Powder, Lyophilized, for Suspension


NDC: 0270-7097
Labeler: Bracco Diagnostics Inc
Product Type: Human Prescription Drug
Drug Name:  Lumason
Dosage Form: Intravenous; Intravesical Injection, Powder, Lyophilized, for Suspension
Application #: NDA203684
Rev. Date: 


NDC Package Codes:

  • 0270-7097-07: 20 VIAL IN 1 BOX (0270‑7097‑07) > 25 MG IN 1 VIAL
  • 0270-7097-08: 20 VIAL IN 1 BOX (0270‑7097‑08) > 25 MG IN 1 VIAL

Active Ingredients:

  • Sulfur Hexafluoride
  • Distearoylphosphatidylcholine
  • Dl-
  • Sodium 1,2-dipalmitoyl-sn-glycero-3-phospho-(1'-rac-glycerol)

Dosage Strength:

  • 60.7 mg/mg
  • .19 mg/mg
  • .19 mg/mg

Pharmaceutical Classes:

  • Contrast Agent for Ultrasound Imaging [EPC]
  • Ultrasound Contrast Activity [MoA]

Related Products:

Based on records with the same trade name.
  • 0270-7099 Lumason Kit by Bracco Diagnostics Inc
  • 68155-099 LumasonLumason Kit by Bracco Suisse Sa

NDC QR Code

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NDC 0270-7097 QR Code

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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.