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
- Bryant Ranch Prepack
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 6d189e86-4c36-43f5-b406-a342458d4155
- SPL ID
- 840d6421-5e3e-4933-84fb-e5676439b9a0
- Version
- 4
- Effective date
- 2020-05-27
- Source export date
- 2026-09-28
- Source partition
- 9
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0009-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/6784607726c827491ceaeab30d843632e0660ee8008c535197be5ed9e1e52201/drug-label-0009-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:03:13
| 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 | Bryant Ranch Prepack | openfda.manufacturer_name | |
| ndc | package | 71335-1396-0 | openfda.package_ndc |
| ndc | package | 71335-1396-3 | openfda.package_ndc |
| ndc | package | 71335-1503-3 | openfda.package_ndc |
| ndc | package | 71335-1396-1 | openfda.package_ndc |
| ndc | package | 71335-1517-8 | openfda.package_ndc |
| ndc | package | 71335-1503-1 | openfda.package_ndc |
| ndc | package | 71335-1503-8 | openfda.package_ndc |
| ndc | package | 71335-1396-6 | openfda.package_ndc |
| ndc | package | 71335-1396-2 | openfda.package_ndc |
| ndc | package | 71335-1503-7 | openfda.package_ndc |
| ndc | package | 71335-1396-4 | openfda.package_ndc |
| ndc | package | 71335-1517-9 | openfda.package_ndc |
| ndc | package | 71335-1517-1 | openfda.package_ndc |
| ndc | package | 71335-1396-5 | openfda.package_ndc |
| ndc | package | 71335-1503-2 | openfda.package_ndc |
| ndc | package | 71335-1396-7 | openfda.package_ndc |
| ndc | package | 71335-1517-2 | openfda.package_ndc |
| ndc | package | 71335-1517-3 | openfda.package_ndc |
| ndc | package | 71335-1517-4 | openfda.package_ndc |
| ndc | package | 71335-1503-0 | openfda.package_ndc |
| ndc | package | 71335-1503-6 | openfda.package_ndc |
| ndc | package | 71335-1517-7 | openfda.package_ndc |
| ndc | package | 71335-1396-9 | openfda.package_ndc |
| ndc | package | 71335-1503-9 | openfda.package_ndc |
| ndc | package | 71335-1517-5 | openfda.package_ndc |
| ndc | package | 71335-1503-5 | openfda.package_ndc |
| ndc | package | 71335-1517-6 | openfda.package_ndc |
| ndc | package | 71335-1396-8 | openfda.package_ndc |
| ndc | package | 71335-1503-4 | openfda.package_ndc |
| ndc | product | 71335-1396 | openfda.product_ndc |
| ndc | product | 71335-1503 | openfda.product_ndc |
| ndc | product | 71335-1517 | openfda.product_ndc |
| ndc11 | package | 71335139605 | derived:openfda.package_ndc |
| ndc11 | package | 71335151705 | derived:openfda.package_ndc |
| ndc11 | package | 71335139601 | derived:openfda.package_ndc |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.