Erlotinib

SPL

Last synced from FDA National Drug Code directory (United States) on June 3, 2026

Identification

ManufacturerTeva Pharmaceuticals USA, Inc.

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
0093766356
30 TABLET, FILM COATED in 1 BOTTLE (0093-7663-56)

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Raw payload (JSON)

{
  "route": "ORAL",
  "productid": "0093-7663_4368f7b2-5bdb-4232-90b0-f6a769d71e9b",
  "productndc": "0093-7663",
  "dosage_form": "TABLET, FILM COATED",
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "ERLOTINIB HYDROCHLORIDE",
  "proprietary_name": "Erlotinib",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA091059",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Erlotinib",
  "start_marketing_date": "20190509",
  "active_numerator_strength": "100"
}

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