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Erlotinib

NDC 72485-219, Erlotinib hydrochloride, tablet, film coated, from Armas Pharmaceuticals Inc..

Product NDC
72485-219
Status
Listed
Labeler
Armas Pharmaceuticals Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA211960
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/72485-219 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • ERLOTINIB HYDROCHLORIDE150 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
72485-219-30724850219301 BOTTLE in 1 BOX (72485-219-30) / 30 TABLET, FILM COATED in 1 BOTTLE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/766baa46-1916-44e8-b599-33017a4194f1

Use it

Look up 72485-219 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/72485-219 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 72485-219. 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.