lumason

Generic: sulfur hexafluoride

Labeler: bracco diagnostics inc
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name lumason
Generic Name sulfur hexafluoride
Labeler bracco diagnostics inc
Dosage Form KIT
Manufacturer
BRACCO DIAGNOSTICS INC

Identifiers & Regulatory

Product NDC 0270-7099
Product ID 0270-7099_47b0f2df-0b6c-a221-750d-763d5ece665b
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA203684
Listing Expiration 2026-12-31
Marketing Start 2020-01-15

Pharmacologic Class

Established (EPC)
contrast agent for ultrasound imaging [epc]
Mechanism of Action
ultrasound contrast activity [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 02707099
Hyphenated Format 0270-7099

Supplemental Identifiers

UNII
EAG959U971 841B886EJ7 WS7LR3I1D6
NUI
N0000175864 N0000010259

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name lumason (source: ndc)
Generic Name sulfur hexafluoride (source: ndc)
Application Number NDA203684 (source: ndc)
Routes
intravenous intravesical
source: label

Resolved Composition

Strengths
  • 25 mg
  • 60.7 mg
  • 5 ml
  • 0.9 %
  • 45 mcg/ml
source: label
Packaging
  • 5 KIT in 1 BOX (0270-7099-73) / 1 KIT in 1 KIT * 25 mg in 1 VIAL * 5 mL in 1 SYRINGE
source: ndc

Packages (1)

0270-7099-73 5 KIT in 1 BOX (0270-7099-73) / 1 KIT in 1 KIT * 25 mg in 1 VIAL * 5 mL in 1 SYRINGE

Ingredients (0)

No ingredient records.

Linked Drug Pages (2)

LumaSon ndc-match (0.9) Lumason, LumaSon ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"spl_id": "47b0f2df-0b6c-a221-750d-763d5ece665b", "openfda": {"nui": ["N0000175864", "N0000010259"], "unii": ["EAG959U971", "841B886EJ7", "WS7LR3I1D6"], "spl_set_id": ["69822a55-226c-f133-e3b8-2b5826667c5b"], "pharm_class_epc": ["Contrast Agent for Ultrasound Imaging [EPC]"], "pharm_class_moa": ["Ultrasound Contrast Activity [MoA]"], "manufacturer_name": ["BRACCO DIAGNOSTICS INC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "5 KIT in 1 BOX (0270-7099-73)  / 1 KIT in 1 KIT *  25 mg in 1 VIAL *  5 mL in 1 SYRINGE", "package_ndc": "0270-7099-73", "marketing_start_date": "20200115"}], "brand_name": "LumaSon", "product_id": "0270-7099_47b0f2df-0b6c-a221-750d-763d5ece665b", "dosage_form": "KIT", "product_ndc": "0270-7099", "generic_name": "SULFUR HEXAFLUORIDE", "labeler_name": "BRACCO DIAGNOSTICS INC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "LumaSon", "application_number": "NDA203684", "marketing_category": "NDA", "marketing_start_date": "20200115", "listing_expiration_date": "20261231"}