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BRUKINSA

NDC 72579-011, zanubrutinib, capsule, from BeOne Medicines USA, Inc..

Product NDC
72579-011
Status
Listed
Labeler
BeOne Medicines USA, Inc.
Dosage form
CAPSULE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA
Application
NDA213217
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/72579-011 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • ZANUBRUTINIB80 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
72579-011-02725790011021 BOTTLE, PLASTIC in 1 CARTON (72579-011-02) / 120 CAPSULE in 1 BOTTLE, PLASTIC

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 72579-011 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/72579-011 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 72579-011. 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.