Active ingredient
Zanubrutinib NDC Codes
Zanubrutinib is an active ingredient in 2 finished products listed with the FDA, under 1 name.
Overview
Each product below links to its own NDC page with package NDCs in 10- and 11-digit form.
- Brand and generic names
- Brukinsa
- Labelers
- BeOne Medicines USA, Inc.
- Strengths
- Zanubrutinib 160 mg/1; Zanubrutinib 80 mg/1
- Dosage forms
- Tablet, Film coated, Capsule
- Routes
- Oral
- Drug classes (FDA established)
- Kinase Inhibitor
- HCPCS / J-code
- None in Med-Code's directory for these products
- Package NDCs
- 2
NDC codes
Newest listings first. Each row links to the product’s NDC page.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) | HCPCS |
|---|---|---|---|---|---|---|
| Brukinsazanubrutinib | Zanubrutinib 160 mg/1 | Tablet, Film coatedOral | BeOne Medicines USA, Inc. | 72579-122 | 72579-0122-01 | — |
| Brukinsazanubrutinib | Zanubrutinib 80 mg/1 | CapsuleOral | BeOne Medicines USA, Inc. | 72579-011 | 72579-0011-02 | — |
Zanubrutinib: common questions
- Which drugs contain Zanubrutinib?
- Brukinsa.
- Is there a J-code for Zanubrutinib?
- Med-Code's curated HCPCS directory has no drug-specific code for these products. Drugs dispensed by a pharmacy are billed by NDC. NDC vs J-code.
- Which NDC goes on a claim?
- The package NDC of what was given, in 11-digit form. How to convert a 10-digit NDC.