Prescription drug · NDA
Brukinsa (zanubrutinib) NDC 72579-122
Zanubrutinib 160 mg/1 · Tablet, Film coated · Oral · BeOne Medicines USA, Inc.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 72579-122-01 | 72579012201 | 1 BOTTLE in 1 CARTON (72579-122-01) / 60 TABLET, FILM COATED in 1 BOTTLEMarketed from Aug 18, 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)
- Brukinsa
- Generic name (nonproprietary)
- zanubrutinib
- Active ingredients
- Zanubrutinib — 160 mg/1
- Dosage form
- Tablet, Film coated
- Route
- Oral
- Labeler
- BeOne Medicines USA, Inc.
- Product type
- Prescription drug
- Marketing category
- NDA — New Drug ApplicationApplication NDA 218785
- Marketing start
- Listing expires
- Other FDA classes
- Bruton's Tyrosine Kinase Inhibitors (Mechanism)
- Identifiers
- Product ID 72579-122_23c53429-0c0d-4acc-bdee-3ed47625db4aSPL ID 23c53429-0c0d-4acc-bdee-3ed47625db4a
- Pharmacologic class
- Kinase Inhibitor
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
N472579012201followed by a unit qualifier and the quantityPackage 72579-0122-01. 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.