IBUPROFEN
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
- IBUPROFEN
- Generic name
- IBUPROFEN
- Manufacturer
- DIRECT RX
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- c3f30813-0848-6e8a-e053-2995a90a3dea
- SPL ID
- 2c285455-94b8-8154-e063-6394a90a0e8c
- Version
- 11
- Effective date
- 2025-01-20
- Source export date
- 2026-09-28
- Source partition
- 4
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:24:50
| 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 | 090796 | derived:openfda.application_number |
| application number | ANDA090796 | openfda.application_number | |
| brand name | IBUPROFEN | openfda.brand_name | |
| generic name | IBUPROFEN | openfda.generic_name | |
| manufacturer name | DIRECT RX | openfda.manufacturer_name | |
| ndc | package | 72189-231-90 | openfda.package_ndc |
| ndc | package | 72189-266-71 | openfda.package_ndc |
| ndc | package | 72189-231-60 | openfda.package_ndc |
| ndc | package | 72189-231-21 | openfda.package_ndc |
| ndc | package | 72189-266-72 | openfda.package_ndc |
| ndc | package | 72189-266-90 | openfda.package_ndc |
| ndc | package | 72189-266-60 | openfda.package_ndc |
| ndc | package | 72189-231-30 | openfda.package_ndc |
| ndc | package | 72189-266-15 | openfda.package_ndc |
| ndc | package | 72189-266-30 | openfda.package_ndc |
| ndc | package | 72189-266-40 | openfda.package_ndc |
| ndc | product | 72189-266 | openfda.product_ndc |
| ndc | product | 72189-231 | openfda.product_ndc |
| ndc11 | package | 72189026640 | derived:openfda.package_ndc |
| ndc11 | package | 72189026672 | derived:openfda.package_ndc |
| ndc11 | package | 72189023190 | derived:openfda.package_ndc |
| ndc11 | package | 72189026690 | derived:openfda.package_ndc |
| ndc11 | package | 72189023121 | derived:openfda.package_ndc |
| ndc11 | package | 72189026630 | derived:openfda.package_ndc |
| ndc11 | package | 72189026660 | derived:openfda.package_ndc |
| ndc11 | package | 72189026671 | derived:openfda.package_ndc |
| ndc11 | package | 72189026615 | derived:openfda.package_ndc |
| ndc11 | package | 72189023160 | derived:openfda.package_ndc |
| ndc11 | package | 72189023130 | derived:openfda.package_ndc |
| rxcui | 197807 | openfda.rxcui | |
| rxcui | 197806 | openfda.rxcui | |
| spl id | 2c285455-94b8-8154-e063-6394a90a0e8c | id | |
| spl set id | c3f30813-0848-6e8a-e053-2995a90a3dea | set_id | |
| unii | WK2XYI10QM | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.