Nelarabine
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
- Nelarabine
- Generic name
- NELARABINE
- Manufacturer
- Zydus Lifesciences Limited
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 877b69a0-0899-455d-926e-f5a7478c31f8
- SPL ID
- d96809f2-f942-4f6d-92b9-0a23ec84226d
- Version
- 2
- Effective date
- 2022-11-05
- Source export date
- 2026-10-22
- Source partition
- 8
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-22/0bafccaf0213baa649cda9c1c2365d28432e10cf46f4167b2ea41290b5cac2b8/drug-label-0008-of-0014.json.zip
- Source manifest SHA-256
- 5de9d3c3492926d1703b492ae4d29b036ac5be73edfcb92a6cd5eb95a2acef9c
- Import run
- 20261023T001338Z
- Imported at
- 2026-10-23 00:59:30
| Harmonized routes |
|---|
| INTRAVENOUS |
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 | 215037 | derived:openfda.application_number |
| application number | ANDA215037 | openfda.application_number | |
| brand name | Nelarabine | openfda.brand_name | |
| generic name | NELARABINE | openfda.generic_name | |
| manufacturer name | Zydus Lifesciences Limited | openfda.manufacturer_name | |
| ndc | package | 70771-1685-1 | openfda.package_ndc |
| ndc | package | 70771-1685-8 | openfda.package_ndc |
| ndc | product | 70771-1685 | openfda.product_ndc |
| ndc11 | package | 70771168501 | derived:openfda.package_ndc |
| ndc11 | package | 70771168508 | derived:openfda.package_ndc |
| rxcui | 603566 | openfda.rxcui | |
| spl id | d96809f2-f942-4f6d-92b9-0a23ec84226d | id | |
| spl set id | 877b69a0-0899-455d-926e-f5a7478c31f8 | set_id | |
| unii | 60158CV180 | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.