NDC codes

FDA NDC Directory
Product NDC (as listed)0270-7099Labeler and product segments. Claims need a package NDC.
Product NDC at billing width00270-7099Add the package segment from the table below.
Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC11-digit (billing)PackageCopy
0270-7099-7300270709973002707099735 KIT in 1 BOX (0270-7099-73) / 1 KIT in 1 KIT * 25 mg in 1 VIAL * 5 mL in 1 SYRINGEMarketed from Jan 15, 2020

How the 11-digit form is made: The labeler segment has 4 digits, so one leading zero is added to it (4-4-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary)
LumaSon
Generic name (nonproprietary)
sulfur hexafluoride
Dosage form
Kit
Labeler
BRACCO DIAGNOSTICS INCNDC labeler code 0270
Product type
Prescription drug
Marketing category
NDA — New Drug ApplicationApplication NDA 203684
Marketing start
Listing expires
Identifiers
Product ID 0270-7099_52f1ae95-1fe4-40dc-8e57-203664301db8SPL ID 52f1ae95-1fe4-40dc-8e57-203664301db8

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.

NDC on a medical claim

N400270709973 followed by a unit qualifier and the quantity

Package 00270-7099-73. 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 0270-7099

What is NDC 0270-7099?
0270-7099 is the product NDC for LumaSon (sulfur hexafluoride) kit, 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).
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.

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

Other LumaSon NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Lumasonsulfur hexafluorideSulfur hexafluoride 60.7 mg/mg + 2 more ingredientsInjection, Powder, Lyophilized, For suspensionIntravenous, IntravesicalBRACCO DIAGNOSTICS INC0270-709700270-7097-08

Other NDCs under NDA 203684

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

FDA NDC Directory listings under NDA 203684
ProductStrengthForm · routeLabelerProduct NDC
Lumasonsulfur hexafluorideSulfur hexafluoride 60.7 mg/mg + 2 more ingredientsInjection, Powder, Lyophilized, For suspensionIntravenous, IntravesicalBRACCO DIAGNOSTICS INC0270-7097

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