NDC 80425-0089-01 - Ibuprofen
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 80425-0089
- Requested NDC
- 80425-0089-01
- Package NDCs from labels
- 80425-0089-4, 80425-0089-1, 80425-0089-2, 80425-0089-3, 80425-0089-01
- Manufacturer
- Advanced Rx of Tennessee, LLC
- Effective date
- 2024-12-31
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Ibuprofen - Advanced Rx of Tennessee, LLC | Advanced Rx of Tennessee, LLC | 2024-12-31 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 80425-0089-1 | Ibuprofen | 30 in 1 BOTTLE | TABLET, FILM COATED | 30 | 10 | |
| 80425-0089-2 | Ibuprofen | 90 in 1 BOTTLE | TABLET, FILM COATED | 90 | 10 | |
| 80425-0089-3 | Ibuprofen | 120 in 1 BOTTLE | TABLET, FILM COATED | 120 | 10 | |
| 80425-0089-4 | Ibuprofen | 60 in 1 BOTTLE | TABLET, FILM COATED | 60 | 10 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 80425-0089 | IBUPROFEN TABLET, FILM COATED [ADVANCED RX OF TENNESSEE, LLC] | 10 | Current NDC, Legacy NDC, 4 package rows | 20250101_b33caad1-8d40-16f2-e053-2a95a90a1b2d.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 80425-0089-1 | EA - Each | 80425-0089 | 01ce4c5e-17ef-4f4b-b965-568a87abebf1 | 1 | 2023-06-06 |
| 80425-0089-2 | EA - Each | 80425-0089 | 6ac60d16-43c1-486a-a4a2-aeae77dad7cb | 1 | 2023-06-06 |
| 80425-0089-3 | EA - Each | 80425-0089 | f137aff3-c81c-4c4d-ab0a-27b16fd37c15 | 1 | 2023-06-06 |
| 80425-0089-4 | EA - Each | 80425-0089 | f74fc782-5cf4-468d-8455-425ded548afa | 1 | 2023-06-06 |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Pain Reliever | ACETAMINOPHEN, IBUPROFEN | CVS Pharmacy | 9126e680-d5ff-4189-9f9a-d797822ce670 | 2026-08-26 | Warnings | WK2XYI10QM |
| Leader Dual Action Pain Reliever | ACETAMINOPHEN, IBUPROFEN | Cardinal Health 110, LLC. dba Leader | 2bb1f616-48af-4fe1-9aa9-32fcb2dba50c | 2026-08-26 | Warnings | WK2XYI10QM |
| dual pain reliever | ACETAMINOPHEN, IBUPROFEN | Walgreen Company | 5cb3b0b4-5b47-4ed4-a5e3-f14dbbcb46df | 2026-08-26 | Warnings | WK2XYI10QM |
| Infants Ibuprofen | IBUPROFEN | Walgreens | 3bbbe142-a00c-404b-a116-81ad730ea130 | 2026-08-25 | Warnings | WK2XYI10QM |
| Ibuprofen | IBUPROFEN | Major Pharmaceuticals | ba86e936-ef72-43e5-aebf-f2c788fe2266 | 2026-08-20 | Boxed warning, Warnings, Adverse reactions | 197805 197807 197806 WK2XYI10QM |
| Combogesic | ACETAMINOPHEN AND IBUPROFEN | Preferred Pharmaceuticals Inc. | f3cee991-19ef-4a1c-bb14-cbc8b6f32776 | 2026-08-20 | Boxed warning, Warnings, Adverse reactions | WK2XYI10QM |
| Ibuprofen | IBUPROFEN | Safeway, Inc. | 57f06daf-690d-44a7-95a5-468732949750 | 2026-08-19 | Warnings | WK2XYI10QM |
| ibuprofen | IBUPROFEN | NuCare Pharmaceuticals,Inc. | 59554a62-3a9a-c0f3-e063-6294a90ad3fd | 2026-08-18 | Warnings | WK2XYI10QM |
| CHILDRENS IBUPROFEN | IBUPROFEN | Amazon.com Services LLC | 0865fe8a-df81-4ae4-8bed-29a022ba164f | 2026-08-17 | Warnings | WK2XYI10QM |
| CHILDRENS IBUPROFEN | IBUPROFEN | Amazon.com Services LLC | 5ba08c30-7eb9-433b-b763-9288f4dd1012 | 2026-08-12 | Warnings | WK2XYI10QM |
| Ibuprofen PM | DIPHENHYDRAMINE CITRATE, IBUPROFEN | WALMART INC. (see also Equate) | d86151b6-d5c5-4d93-9cfd-43ab7ad0443a | 2026-08-12 | Warnings | WK2XYI10QM |
| Ibuprofen | IBUPROFEN | AiPing Pharmaceutical, Inc. | 3e131710-2579-446e-8076-f602ecea813f | 2026-08-11 | Boxed warning, Warnings, Adverse reactions | 197805 197807 197806 WK2XYI10QM |
| INFANTS IBUPROFEN | IBUPROFEN | Amazon.com Services LLC | 8588617a-d4b8-4ab5-8b87-30e6f1121cc3 | 2026-08-10 | Warnings | WK2XYI10QM |
| Ibuprofen | IBUPROFEN | Shield Pharmaceuticals Corp | 22102461-0196-4ef0-aef4-66997d74d118 | 2026-08-10 | Warnings | WK2XYI10QM |
| Ibuprofen minis | IBUPROFEN | Walgreens | 6d1d131d-0741-4a75-8383-9322f4f3faab | 2026-08-06 | Warnings | WK2XYI10QM |
| Ibuprofen | IBUPROFEN | Shield Pharmaceuticals Corp | 216e5600-56b4-44b0-88b7-69adfb245802 | 2026-08-06 | Warnings | WK2XYI10QM |
| Ibuprofen | IBUPROFEN | COSTCO WHOLESALE CORPORATION | 4b8ad98e-de76-4f49-3b89-01e9dd5cde16 | 2026-08-06 | Warnings | WK2XYI10QM |
| Dye Free Ibuprofen | IBUPROFEN | Walgreen Company | d3d093f9-207a-40d4-a7be-c6b5a544a0a7 | 2026-08-06 | Warnings | WK2XYI10QM |
| Ibuprofen | IBUPROFEN | P & L Development, LLC | 159b68b7-54e5-4f83-b632-f49e7b4b14a5 | 2026-08-05 | Warnings | WK2XYI10QM |
| Ibuprofen | IBUPROFEN | Walgreen Company | c118b290-f821-4e73-906e-8a93edaf34e4 | 2026-08-05 | Warnings | WK2XYI10QM |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.