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BRUKINSA

NDC 72579-122, zanubrutinib, tablet, film coated, from BeOne Medicines USA, Inc..

Product NDC
72579-122
Status
Listed
Labeler
BeOne Medicines USA, Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA
Application
NDA218785
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/72579-122 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • ZANUBRUTINIB160 mg/1

Pharmacologic classes

Bruton's Tyrosine Kinase Inhibitors [MoA]; Kinase Inhibitor [EPC]

Package NDCNDC-11Package
72579-122-01725790122011 BOTTLE in 1 CARTON (72579-122-01) / 60 TABLET, FILM COATED in 1 BOTTLE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/3e08fe23-d70e-424c-bc51-1222e320f902

Use it

Look up 72579-122 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/72579-122 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 72579-122. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.