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
- NuCare Pharmaceuticals,Inc.
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 9b02607a-6fab-5205-e053-2a95a90afa26
- SPL ID
- 2abe1780-d1e5-a90a-e063-6294a90a64ee
- Version
- 6
- Effective date
- 2025-01-02
- Source export date
- 2026-09-28
- 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/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:57:37
| 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 | NuCare Pharmaceuticals,Inc. | openfda.manufacturer_name | |
| ndc | package | 68071-5140-3 | openfda.package_ndc |
| ndc | package | 68071-5140-6 | openfda.package_ndc |
| ndc | product | 68071-5140 | openfda.product_ndc |
| ndc11 | package | 68071514006 | derived:openfda.package_ndc |
| ndc11 | package | 68071514003 | derived:openfda.package_ndc |
| rxcui | 197807 | openfda.rxcui | |
| spl id | 2abe1780-d1e5-a90a-e063-6294a90a64ee | id | |
| spl set id | 9b02607a-6fab-5205-e053-2a95a90afa26 | set_id | |
| unii | WK2XYI10QM | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.