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Lapatinib

NDC 42291-035, Lapatinib, tablet, film coated, from AvKARE.

Product NDC
42291-035
Status
Listed
Labeler
AvKARE
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA217968
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/42291-035 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • LAPATINIB DITOSYLATE250 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
42291-035-1542291003515150 TABLET, FILM COATED in 1 BOTTLE (42291-035-15)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/302a4346-a68d-af3e-e063-6294a90a4a6f

Use it

Look up 42291-035 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/42291-035 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 42291-035. 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.