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Erlotinib Hydrochloride

NDC 72205-081, Erlotinib Hydrochloride, tablet, film coated, from Novadoz Pharmaceuticals LLC.

Product NDC
72205-081
Status
Listed
Labeler
Novadoz Pharmaceuticals LLC
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA214366
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/72205-081 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • ERLOTINIB HYDROCHLORIDE100 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
72205-081-30722050081301 BOTTLE in 1 CARTON (72205-081-30) / 30 TABLET, FILM COATED in 1 BOTTLE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/4cff04f5-3693-4d87-a9f8-a2b195e3d26e

Use it

Look up 72205-081 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/72205-081 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 72205-081. 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.