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Erlotinib

NDC 70771-1521, Erlotinib, tablet, film coated, from Zydus Lifesciences Limited.

Product NDC
70771-1521
Status
Listed
Labeler
Zydus Lifesciences Limited
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA213065
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70771-1521 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • ERLOTINIB HYDROCHLORIDE25 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
70771-1521-37077115210330 TABLET, FILM COATED in 1 BOTTLE (70771-1521-3)
70771-1521-7707711521073 BLISTER PACK in 1 CARTON (70771-1521-7) / 10 TABLET, FILM COATED in 1 BLISTER PACK (70771-1521-2)
70771-1521-97077115210990 TABLET, FILM COATED in 1 BOTTLE (70771-1521-9)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/daaa1329-3a3f-439c-b13d-b301daa234d4

Use it

Look up 70771-1521 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70771-1521 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70771-1521. 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.