DOXORUBICIN HYDROCHLORIDE
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
- DOXORUBICIN HYDROCHLORIDE
- Generic name
- DOXORUBICIN HYDROCHLORIDE
- Manufacturer
- Zydus Lifesciences Limited
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- bad467d4-7e27-4eda-b4d3-854460f0adab
- SPL ID
- 2c0f5abf-ca66-445c-9a35-e39b2111911e
- Version
- 2
- Effective date
- 2022-11-01
- Source export date
- 2026-10-27
- Source partition
- 5
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-27/35717de05250cd386420cc8ede3b6010b48d18eea2af59afb0617fcabca634ec/drug-label-0005-of-0014.json.zip
- Source manifest SHA-256
- 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
- Import run
- 20261027T193451Z
- Imported at
- 2026-10-27 20:04:19
| 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 | 212299 | derived:openfda.application_number |
| application number | ANDA212299 | openfda.application_number | |
| brand name | DOXORUBICIN HYDROCHLORIDE | openfda.brand_name | |
| generic name | DOXORUBICIN HYDROCHLORIDE | openfda.generic_name | |
| manufacturer name | Zydus Lifesciences Limited | openfda.manufacturer_name | |
| ndc | package | 49315-008-03 | openfda.package_ndc |
| ndc | package | 49315-009-07 | openfda.package_ndc |
| ndc | product | 49315-009 | openfda.product_ndc |
| ndc | product | 49315-008 | openfda.product_ndc |
| ndc11 | package | 49315000907 | derived:openfda.package_ndc |
| ndc11 | package | 49315000803 | derived:openfda.package_ndc |
| rxcui | 1790127 | openfda.rxcui | |
| rxcui | 1790115 | openfda.rxcui | |
| spl id | 2c0f5abf-ca66-445c-9a35-e39b2111911e | id | |
| spl set id | bad467d4-7e27-4eda-b4d3-854460f0adab | set_id | |
| unii | 82F2G7BL4E | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.