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BOSULIF

NDC 63539-193, Bosutinib, tablet, film coated, from U.S. Pharmaceuticals.

Product NDC
63539-193
Status
Listed
Labeler
U.S. Pharmaceuticals
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA
Application
NDA203341
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/63539-193 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • BOSUTINIB MONOHYDRATE400 mg/1

Pharmacologic classes

Bcr-Abl Tyrosine Kinase Inhibitors [MoA]; Kinase Inhibitor [EPC]

Package NDCNDC-11Package
63539-193-306353901933030 TABLET, FILM COATED in 1 BOTTLE (63539-193-30)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/d5929f91-6496-4c0e-97e8-0bd524e15763

Use it

Look up 63539-193 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/63539-193 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 63539-193. 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.