NDC 80425-0046-01 - 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
- 80425-0046
- Requested NDC
- 80425-0046-01
- Package NDCs from labels
- 80425-0046-3, 80425-0046-1, 80425-0046-2, 80425-0046-4, 80425-0046-5, 80425-0046-01
- Manufacturer
- Advanced Rx of Tennessee, LLC
- Effective date
- 2025-08-07
- 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 | 2025-08-07 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 80425-0046-1 | Ibuprofen | 90 in 1 BOTTLE | TABLET, FILM COATED | 90 | 10 | |
| 80425-0046-2 | Ibuprofen | 120 in 1 BOTTLE | TABLET, FILM COATED | 120 | 10 | |
| 80425-0046-3 | Ibuprofen | 60 in 1 BOTTLE | TABLET, FILM COATED | 60 | 10 | |
| 80425-0046-4 | Ibuprofen | 30 in 1 BOTTLE | TABLET, FILM COATED | 30 | 10 | |
| 80425-0046-5 | Ibuprofen | 100 in 1 BOTTLE | TABLET, FILM COATED | 100 | 10 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 80425-0046 | IBUPROFEN TABLET, FILM COATED [ADVANCED RX OF TENNESSEE, LLC] | 9 | Current NDC, Legacy NDC, 5 package rows | 20250101_af9ac948-440c-5abf-e053-2995a90af2b5.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 80425-0046-1 | EA - Each | 80425-0046 | 62581d8b-2f74-46b8-863f-a79f6a44d7a5 | 1 | 2023-06-06 |
| 80425-0046-2 | EA - Each | 80425-0046 | 155f2633-4c11-401d-b550-262b6ca9e2c5 | 1 | 2023-06-06 |
| 80425-0046-3 | EA - Each | 80425-0046 | 4fdfb716-6522-430f-a2ba-d234476a5686 | 1 | 2023-06-06 |
| 80425-0046-4 | EA - Each | 80425-0046 | c97f3641-cd80-4bf6-9b61-25a0bd8be5a9 | 1 | 2023-06-06 |
| 80425-0046-5 | EA - Each | 80425-0046 | 4b9256f5-33f7-42a3-86fb-30d523c705b6 | 1 | 2025-09-12 |
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 |
|---|---|---|---|---|---|---|
| Advil | IBUPROFEN | Haleon US Holdings LLC | 1f01c10a-9434-91a4-2ee4-352315a6b610 | 2026-07-29 | Warnings | WK2XYI10QM |
| Ibuprofen and famotidine | IBUPROFEN AND FAMOTIDINE | Ascend Laboratories, LLC | 4493d4cd-ca8e-4b0a-9b65-b75e55bf8b9e | 2026-07-28 | Boxed warning, Warnings, Adverse reactions | WK2XYI10QM |
| Ibuprofen | IBUPROFEN | H E B | 21567c0f-abba-4a40-a0b9-5ce49b3d9648 | 2026-07-28 | Warnings | WK2XYI10QM |
| Ibuprofen | IBUPROFEN | PD-Rx Pharmaceuticals, Inc. | 656658cc-8cf0-42b6-af4f-4e3ab7648625 | 2026-07-27 | Boxed warning, Warnings, Adverse reactions | 197807 WK2XYI10QM |
| Ibuprofen | IBUPROFEN | REMEDYREPACK INC. | a7756b22-73cf-4262-aa8e-0577ddecd03b | 2026-07-24 | Boxed warning, Warnings, Adverse reactions | 197805 WK2XYI10QM |
| Ibuprofen | IBUPROFEN | Shield Pharmaceuticals Corp | 1ca722bb-940e-4b3e-9561-d87e2feb1ff8 | 2026-07-24 | Warnings | WK2XYI10QM |
| Ibuprofen | IBUPROFEN | Shield Pharmaceuticals Corp | fc6c29b4-f1b3-4cfe-8c96-564d083be39c | 2026-07-24 | Warnings | WK2XYI10QM |
| childrens ibuprofen | IBUPROFEN | Rite Aid Corporation | 26bccfc1-bc8d-4241-a078-c760048951c9 | 2026-07-24 | Warnings | WK2XYI10QM |
| IBUPROFEN | IBUPROFEN | HF Acquisition Co LLC, DBA HealthFirst | 574b6f15-70bc-fca7-e063-6294a90a0455 | 2026-07-23 | Warnings | WK2XYI10QM |
| Ibuprofen | IBUPROFEN | Safeway, Inc. | a530d43d-e9c4-4edb-af66-c92860e46f45 | 2026-07-23 | Warnings | WK2XYI10QM |
| Ibuprofen | IBUPROFEN | TWIN MED LLC | f03958f8-aeae-edf0-e053-2a95a90a3e9e | 2026-07-22 | Warnings | WK2XYI10QM |
| Good Sense ibuprofen | IBUPROFEN | L. Perrigo Company | aebae4b3-18c8-4ecf-b578-1fe7cc50076b | 2026-07-22 | Warnings | WK2XYI10QM |
| Ibuprofen | IBUPROFEN | PD-Rx Pharmaceuticals, Inc. | d3a7ebef-f7ab-4b34-b62e-278a8deabf78 | 2026-07-21 | Boxed warning, Warnings, Adverse reactions | ANDA091625 197806 WK2XYI10QM |
| Ibuprofen | IBUPROFEN | PD-Rx Pharmaceuticals, Inc. | b81c6495-8b30-41ef-8a0f-4cbfd87f1eb4 | 2026-07-21 | Boxed warning, Warnings, Adverse reactions | ANDA091625 197807 WK2XYI10QM |
| Ibuprofen | IBUPROFEN | PD-Rx Pharmaceuticals, Inc. | 0cb73c19-a7cb-4ad9-9aa5-c24afb80d6d8 | 2026-07-20 | Boxed warning, Warnings, Adverse reactions | ANDA091625 197807 WK2XYI10QM |
| Acetaminophen and Ibuprofen | ACETAMINOPHEN AND IBUPROFEN | CVS Pharmacy | 52193849-d03a-b61b-e063-6394a90ad277 | 2026-07-20 | Warnings | WK2XYI10QM |
| good sense dual action | ACETAMINOPHEN, IBUPROFEN | L Perrigo Company | b117358c-f4ca-4ea8-95ee-88a42cc05040 | 2026-07-17 | Warnings | WK2XYI10QM |
| Ibuprofen | IBUPROFEN | REMEDYREPACK INC. | 57a1bf99-5aaf-432d-86ba-5f0e7cfab1a0 | 2026-07-17 | Boxed warning, Warnings, Adverse reactions | ANDA091625 197807 WK2XYI10QM |
| ibuprofen | IBUPROFEN | HyVee Inc | e7175dc9-db39-4452-a419-85af179de422 | 2026-07-16 | Warnings | WK2XYI10QM |
| ibuprofen | IBUPROFEN | Sun Pharmaceutical Industries, Inc. | 9de61620-6750-4fb6-89a4-fe451ab8d99f | 2026-07-15 | Warnings | WK2XYI10QM |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.