NDC codes

FDA NDC Directory
Product NDC (as listed)71558-001Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71558-0001Add 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
71558-001-307155800013030 TABLET in 1 BOTTLE (71558-001-30)Marketed from Aug 12, 2025

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 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)
Brinsupri
Generic name (nonproprietary)
brensocatib
Active ingredients
Brensocatib — 10 mg/1
Dosage form
Tablet
Route
Oral
Labeler
Insmed IncorporatedNDC labeler code 71558
Product type
Prescription drug
Marketing category
NDA — New Drug ApplicationApplication NDA 217673
Marketing start
Listing expires
Identifiers
Product ID 71558-001_43046e5b-e40b-423d-a98d-a2fecc2cbd2eSPL ID 43046e5b-e40b-423d-a98d-a2fecc2cbd2eSPL set ID b56986ae-e7db-421e-b622-a7f41e321f3dRxCUI 2721885, 2721891, 2721893, 2721895UNII 25CG88L0BB

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 HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N471558000130 followed by a unit qualifier and the quantity

Package 71558-0001-30. 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

Current FDA label (SPL), effective .

Indications (excerpt from the label)

BRINSUPRI is indicated for the treatment of non-cystic fibrosis bronchiectasis (NCFB) in adult and pediatric patients 12 years of age and older. BRINSUPRI is a dipeptidyl peptidase 1 (DPP1) inhibitor indicated for the treatment of non-cystic fibrosis bronchiectasis in adult and pediatric patients 12 years of age and older. ( 1 )

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 71558-001

What is NDC 71558-001?
71558-001 is the product NDC for Brinsupri (brensocatib), Brensocatib 10 mg/1 tablet, listed with the FDA by Insmed Incorporated. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Brinsupri (Brensocatib).
What is the active ingredient?
Brensocatib.
Who is the labeler?
Insmed Incorporated, NDC labeler code 71558. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Brinsupri?
1 other product NDC are listed under this name. See all Brinsupri 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 Brinsupri NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
BrinsupribrensocatibBrensocatib 25 mg/1TabletOralInsmed Incorporated71558-00271558-0002-30

Other NDCs under NDA 217673

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

FDA NDC Directory listings under NDA 217673
ProductStrengthForm · routeLabelerProduct NDC
BrinsupribrensocatibBrensocatib 25 mg/1TabletOralInsmed Incorporated71558-002

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