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Gefitinib

NDC 0480-4053, Gefitinib, tablet, film coated, from Teva Pharmaceuticals, Inc..

Product NDC
0480-4053
Status
Listed
Labeler
Teva Pharmaceuticals, Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA208913
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0480-4053 \
  -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
0480-4053-560048040535630 TABLET, FILM COATED in 1 BOTTLE (0480-4053-56)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/3dd135f0-5db1-4236-9756-04533b66dc9d

Use it

Look up 0480-4053 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0480-4053 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0480-4053. 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.