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ERLOTINIB

NDC 31722-265, ERLOTINIB, tablet, film coated, from Camber Pharmaceuticals, Inc..

Product NDC
31722-265
Status
Listed
Labeler
Camber Pharmaceuticals, Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA209267
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/31722-265 \
  -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
31722-265-30317220265301 BOTTLE in 1 CARTON (31722-265-30) / 30 TABLET, FILM COATED in 1 BOTTLE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/a3b2d622-b4d5-4819-862b-f8fd3adcec6f

Use it

Look up 31722-265 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/31722-265 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 31722-265. 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.