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Gefitinib

NDC 69339-168, Gefitinib, tablet, film coated, from Natco Pharma USA LLC.

Product NDC
69339-168
Status
Listed
Labeler
Natco Pharma USA LLC
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA212827
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/69339-168 \
  -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
69339-168-036933901680330 TABLET, FILM COATED in 1 BOTTLE (69339-168-03)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/1a3c0ce7-06a1-4e04-9106-14ddb2a866a5

Use it

Look up 69339-168 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/69339-168 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 69339-168. 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.