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
- 54b25106-5580-119d-e054-00144ff88e88
- SPL ID
- 1d7a1de1-b173-b168-e063-6294a90a878c
- Version
- 4
- Effective date
- 2024-07-17
- Source export date
- 2026-09-28
- Source partition
- 12
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/663999d0fe1757c1e2cd13a4799d76d875f663e0bc57701092264ebe7febfc18/drug-label-0012-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:24:32
| 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 | 68071-4009-5 | openfda.package_ndc |
| ndc | package | 68071-4009-3 | openfda.package_ndc |
| ndc | package | 68071-4009-4 | openfda.package_ndc |
| ndc | package | 68071-4009-6 | openfda.package_ndc |
| ndc | package | 68071-4009-7 | openfda.package_ndc |
| ndc | package | 68071-4009-2 | openfda.package_ndc |
| ndc | package | 68071-4009-1 | openfda.package_ndc |
| ndc | package | 68071-4009-9 | openfda.package_ndc |
| ndc | product | 68071-4009 | openfda.product_ndc |
| ndc11 | package | 68071400904 | derived:openfda.package_ndc |
| ndc11 | package | 68071400902 | derived:openfda.package_ndc |
| ndc11 | package | 68071400909 | derived:openfda.package_ndc |
| ndc11 | package | 68071400907 | derived:openfda.package_ndc |
| ndc11 | package | 68071400903 | derived:openfda.package_ndc |
| ndc11 | package | 68071400901 | derived:openfda.package_ndc |
| ndc11 | package | 68071400906 | derived:openfda.package_ndc |
| ndc11 | package | 68071400905 | derived:openfda.package_ndc |
| rxcui | 197806 | openfda.rxcui | |
| spl id | 1d7a1de1-b173-b168-e063-6294a90a878c | id | |
| spl set id | 54b25106-5580-119d-e054-00144ff88e88 | set_id | |
| unii | WK2XYI10QM | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.