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Gefitinib

NDC 50742-366, Gefitinib, tablet, coated, from Ingenus Pharmaceuticals, LLC.

Product NDC
50742-366
Status
Listed
Labeler
Ingenus Pharmaceuticals, LLC
Dosage form
TABLET, COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA211591
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/50742-366 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • GEFITINIB250 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
50742-366-305074203663030 TABLET, COATED in 1 BOTTLE (50742-366-30)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/6402435f-9f6a-4f02-91a2-6267d783fa78

Use it

Look up 50742-366 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/50742-366 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 50742-366. 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.