dasatinib
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
- dasatinib
- Generic name
- DASATINIB
- Manufacturer
- Zydus Lifesciences Limited
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 4eed6b7b-a09d-4d2e-a345-968dd68323bc
- SPL ID
- 571889d7-845d-4fed-8d7d-6470d4d36fa1
- Version
- 1
- Effective date
- 2025-03-04
- Source export date
- 2026-09-28
- Source partition
- 11
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:16:55
| 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 | 218719 | derived:openfda.application_number |
| application number | ANDA218719 | openfda.application_number | |
| brand name | dasatinib | openfda.brand_name | |
| generic name | DASATINIB | openfda.generic_name | |
| manufacturer name | Zydus Lifesciences Limited | openfda.manufacturer_name | |
| ndc | package | 70771-1904-3 | openfda.package_ndc |
| ndc | package | 70771-1902-6 | openfda.package_ndc |
| ndc | package | 70771-1906-3 | openfda.package_ndc |
| ndc | package | 70771-1905-3 | openfda.package_ndc |
| ndc | package | 70771-1901-6 | openfda.package_ndc |
| ndc | package | 70771-1903-6 | openfda.package_ndc |
| ndc | product | 70771-1906 | openfda.product_ndc |
| ndc | product | 70771-1901 | openfda.product_ndc |
| ndc | product | 70771-1903 | openfda.product_ndc |
| ndc | product | 70771-1902 | openfda.product_ndc |
| ndc | product | 70771-1905 | openfda.product_ndc |
| ndc | product | 70771-1904 | openfda.product_ndc |
| ndc11 | package | 70771190306 | derived:openfda.package_ndc |
| ndc11 | package | 70771190106 | derived:openfda.package_ndc |
| ndc11 | package | 70771190503 | derived:openfda.package_ndc |
| ndc11 | package | 70771190603 | derived:openfda.package_ndc |
| ndc11 | package | 70771190403 | derived:openfda.package_ndc |
| ndc11 | package | 70771190206 | derived:openfda.package_ndc |
| rxcui | 643105 | openfda.rxcui | |
| rxcui | 799047 | openfda.rxcui | |
| rxcui | 643109 | openfda.rxcui | |
| rxcui | 1045402 | openfda.rxcui | |
| rxcui | 1045406 | openfda.rxcui | |
| rxcui | 643107 | openfda.rxcui | |
| spl id | 571889d7-845d-4fed-8d7d-6470d4d36fa1 | id | |
| spl set id | 4eed6b7b-a09d-4d2e-a345-968dd68323bc | set_id | |
| unii | RBZ1571X5H | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.