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Imbruvica

NDC 57962-280, Ibrutinib, tablet, film coated, from Pharmacyclics LLC.

Product NDC
57962-280
Status
Listed
Labeler
Pharmacyclics LLC
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA
Application
NDA210563
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/57962-280 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • IBRUTINIB280 mg/1

Pharmacologic classes

Kinase Inhibitor [EPC]; Protein Kinase Inhibitors [MoA]

Package NDCNDC-11Package
57962-280-28579620280281 BLISTER PACK in 1 CARTON (57962-280-28) / 28 TABLET, FILM COATED in 1 BLISTER PACK

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/0dfd0279-ff17-4ea9-89be-9803c71bab44

Use it

Look up 57962-280 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/57962-280 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 57962-280. 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.