Lumason (Sulfur hexafluoride) NDC 0270-7097

Product information

Brand name (proprietary)

Lumason

Generic name (nonproprietary)

sulfur hexafluoride

Active ingredients

Sulfur hexafluoride — 60.7 mg/mgDistearoylphosphatidylcholine, Dl- — .19 mg/mgSodium 1,2-dipalmitoyl-sn-glycero-3-phospho-(1'-rac-glycerol) — .19 mg/mg

Dosage form

Injection, Powder, Lyophilized, For suspension

Route

Intravenous, Intravesical

Labeler

BRACCO DIAGNOSTICS INCNDC labeler code 0270

Product type

Prescription drug

Marketing category

NDA — New Drug ApplicationApplication NDA 203684

Marketing start

Apr 1, 2021

Listing expires

Dec 31, 2027

Other FDA classes

Ultrasound Contrast Activity (Mechanism)

Identifiers

Product ID 0270-7097_52f1ae95-1fe4-40dc-8e57-203664301db8SPL ID 52f1ae95-1fe4-40dc-8e57-203664301db8

Pharmacologic class

Contrast Agent for Ultrasound Imaging

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No drug-specific HCPCS code in Med-Code's directory for this product. The directory is curated and not complete — check the current CMS HCPCS file before billing.

Administration

Drug administration (CPT 96360–96549)

When a clinician administers the drug, the administration is reported separately. Codes in this range cover hydration, therapeutic injections and infusions, and chemotherapy or other complex drug administration. The right code depends on route, duration and drug type, and self-administered drugs are not billed this way.

How CPT relates to drug billing

NDC on a medical claim

N400270709708 followed by a unit qualifier and the quantity Copy

Package 00270-7097-08. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

The FDA listing for this product does not reference a label (SPL) set.

About NDC 0270-7097

What is NDC 0270-7097?

0270-7097 is the product NDC for Lumason (sulfur hexafluoride), Sulfur hexafluoride 60.7 mg/mg + 2 more ingredients injection, powder, lyophilized, for suspension, listed with the FDA by BRACCO DIAGNOSTICS INC. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Lumason (Sulfur hexafluoride).

What is the active ingredient?

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

Who is the labeler?

BRACCO DIAGNOSTICS INC, NDC labeler code 0270. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Lumason?

1 other product NDC are listed under this name. See all Lumason NDCs.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory. See Billing references above.

Related NDCs: other Lumason products

Other finished products listed under the same name: strengths, forms and labelers.

Other NDCs under NDA 203684

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.