Erlotinib
openFDA label record#
This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.
Verified complete openFDA source JSON
- Brand name
- Erlotinib
- Generic name
- ERLOTINIB
- Manufacturer
- Zydus Lifesciences Limited
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- daaa1329-3a3f-439c-b13d-b301daa234d4
- SPL ID
- 9d253beb-cd1f-45df-9b23-c521269d419f
- Version
- 3
- Effective date
- 2024-11-28
- Source export date
- 2026-09-28
- Source partition
- 2
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/f7d2b6e3f8600cd856280ab55a9c6fa54a642647191d164f9d1110e89f3f4097/drug-label-0002-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:15:59
| Harmonized routes |
|---|
| ORAL |
Harmonized identifier links#
Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
| Type | Scope | Identifier | Source field |
|---|---|---|---|
| application applno | ANDA | 213065 | derived:openfda.application_number |
| application number | ANDA213065 | openfda.application_number | |
| brand name | Erlotinib | openfda.brand_name | |
| generic name | ERLOTINIB | openfda.generic_name | |
| manufacturer name | Zydus Lifesciences Limited | openfda.manufacturer_name | |
| ndc | package | 70771-1523-2 | openfda.package_ndc |
| ndc | package | 70771-1521-2 | openfda.package_ndc |
| ndc | package | 70771-1523-7 | openfda.package_ndc |
| ndc | package | 70771-1522-2 | openfda.package_ndc |
| ndc | package | 70771-1521-3 | openfda.package_ndc |
| ndc | package | 70771-1522-9 | openfda.package_ndc |
| ndc | package | 70771-1522-3 | openfda.package_ndc |
| ndc | package | 70771-1523-3 | openfda.package_ndc |
| ndc | package | 70771-1521-9 | openfda.package_ndc |
| ndc | package | 70771-1522-7 | openfda.package_ndc |
| ndc | package | 70771-1523-9 | openfda.package_ndc |
| ndc | package | 70771-1521-7 | openfda.package_ndc |
| ndc | product | 70771-1523 | openfda.product_ndc |
| ndc | product | 70771-1522 | openfda.product_ndc |
| ndc | product | 70771-1521 | openfda.product_ndc |
| ndc11 | package | 70771152309 | derived:openfda.package_ndc |
| ndc11 | package | 70771152109 | derived:openfda.package_ndc |
| ndc11 | package | 70771152103 | derived:openfda.package_ndc |
| ndc11 | package | 70771152209 | derived:openfda.package_ndc |
| ndc11 | package | 70771152303 | derived:openfda.package_ndc |
| ndc11 | package | 70771152207 | derived:openfda.package_ndc |
| ndc11 | package | 70771152307 | derived:openfda.package_ndc |
| ndc11 | package | 70771152302 | derived:openfda.package_ndc |
| ndc11 | package | 70771152102 | derived:openfda.package_ndc |
| ndc11 | package | 70771152107 | derived:openfda.package_ndc |
| ndc11 | package | 70771152203 | derived:openfda.package_ndc |
| ndc11 | package | 70771152202 | derived:openfda.package_ndc |
| rxcui | 603203 | openfda.rxcui | |
| rxcui | 603208 | openfda.rxcui | |
| rxcui | 603206 | openfda.rxcui | |
| spl id | 9d253beb-cd1f-45df-9b23-c521269d419f | id | |
| spl set id | daaa1329-3a3f-439c-b13d-b301daa234d4 | set_id | |
| unii | DA87705X9K | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.