Prescription drug · NDA
Beqalzi (Sonrotoclax) NDC 72579-015
Kit · BeOne Medicines USA, Inc.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 72579-015-04 | 72579001504 | 1 KIT in 1 KIT (72579-015-04) * 11 TABLET, FILM COATED in 1 BLISTER PACK (72579-017-04) * 11 TABLET, FILM COATED in 1 BLISTER PACK (72579-025-04) * 11 TABLET, FILM COATED in 1 BLISTER PACK (72579-022-04) * 11 TABLET, FILM COATED in 1 BLISTER PACK (72579-020-04)Marketed from Aug 31, 2026 |
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)
- Beqalzi
- Generic name (nonproprietary)
- sonrotoclax
- Dosage form
- Kit
- Labeler
- BeOne Medicines USA, Inc.NDC labeler code 72579
- Product type
- Prescription drug
- Marketing category
- NDA — New Drug ApplicationApplication NDA 220711
- Marketing start
- Listing expires
- Identifiers
- Product ID 72579-015_ddc7ae2e-902c-492e-a132-54f7a6ec9d67SPL ID ddc7ae2e-902c-492e-a132-54f7a6ec9d67
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
N472579001504followed by a unit qualifier and the quantityPackage 72579-0015-04. 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 72579-015
- What is NDC 72579-015?
- 72579-015 is the product NDC for Beqalzi (sonrotoclax) kit, listed with the FDA by BeOne Medicines USA, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Beqalzi (Sonrotoclax).
- Who is the labeler?
- BeOne Medicines USA, Inc., NDC labeler code 72579. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Beqalzi?
- 4 other product NDCs are listed under this name. See all Beqalzi NDCs.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
Related NDCs: other Beqalzi products
Other finished products listed under the same name: strengths, forms and labelers.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) |
|---|---|---|---|---|---|
| Beqalzisonrotoclax | Sonrotoclax 5 mg/1 | Tablet, Film coatedOral | BeOne Medicines USA, Inc. | 72579-017 | 72579-0017-01 |
| Beqalzisonrotoclax | Sonrotoclax 1 mg/1 | Tablet, Film coatedOral | BeOne Medicines USA, Inc. | 72579-020 | 72579-0020-01 |
| Beqalzisonrotoclax | Sonrotoclax 80 mg/1 | Tablet, Film coatedOral | BeOne Medicines USA, Inc. | 72579-022 | 72579-0022-0172579-0022-08 |
| Beqalzisonrotoclax | Sonrotoclax 20 mg/1 | Tablet, Film coatedOral | BeOne Medicines USA, Inc. | 72579-025 | 72579-0025-0172579-0025-02 |
Other NDCs under NDA 220711
Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.
| Product | Strength | Form · route | Labeler | Product NDC |
|---|---|---|---|---|
| Beqalzisonrotoclax | Sonrotoclax 5 mg/1 | Tablet, Film coatedOral | BeOne Medicines USA, Inc. | 72579-017 |
| Beqalzisonrotoclax | Sonrotoclax 1 mg/1 | Tablet, Film coatedOral | BeOne Medicines USA, Inc. | 72579-020 |
| Beqalzisonrotoclax | Sonrotoclax 80 mg/1 | Tablet, Film coatedOral | BeOne Medicines USA, Inc. | 72579-022 |
| Beqalzisonrotoclax | Sonrotoclax 20 mg/1 | Tablet, Film coatedOral | BeOne Medicines USA, Inc. | 72579-025 |