NDC 80425-0384-01 - IBUPROFEN AND FAMOTIDINE
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
- 80425-0384
- Requested NDC
- 80425-0384-01
- Package NDCs from labels
- 80425-0384-1, 80425-0384-2, 80425-0384-3, 80425-0384-01
- Manufacturer
- Advanced Rx Pharmacy of Tennessee, LLC
- Effective date
- 2024-04-23
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| IBUPROFEN AND FAMOTIDINE - Advanced Rx Pharmacy of Tennessee, LLC | Advanced Rx Pharmacy of Tennessee, LLC | 2024-04-23 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 80425-0384-1 | IBUPROFEN AND FAMOTIDINE | 30 in 1 BOTTLE | TABLET | 30 | 1 | |
| 80425-0384-2 | IBUPROFEN AND FAMOTIDINE | 60 in 1 BOTTLE | TABLET | 60 | 1 | |
| 80425-0384-3 | IBUPROFEN AND FAMOTIDINE | 90 in 1 BOTTLE | TABLET | 90 | 1 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 80425-0384 | IBUPROFEN AND FAMOTIDINE TABLET [ADVANCED RX PHARMACY OF TENNESSEE, LLC] | 1 | Current NDC, 3 package rows | 20240426_16c8b0db-37d0-99d9-e063-6394a90ac31b.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 80425-0384-1 | EA - Each | 80425-0384 | 76e60705-5101-43cb-8730-11d39c68e1f5 | 1 | 2024-06-10 |
| 80425-0384-2 | EA - Each | 80425-0384 | ccfa16aa-ab0a-4739-bb06-14b214400e27 | 1 | 2024-06-10 |
| 80425-0384-3 | EA - Each | 80425-0384 | 4d802630-9552-417f-ab5b-8a83770799ef | 1 | 2024-06-10 |
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 |
|---|---|---|---|---|---|---|
| Ibuprofen | IBUPROFEN | PD-Rx Pharmaceuticals, Inc. | 656658cc-8cf0-42b6-af4f-4e3ab7648625 | 2026-07-27 | Boxed warning, Warnings, Adverse reactions | WK2XYI10QM |
| Famotidine | FAMOTIDINE | Ascend Laboratories, LLC | b2228be0-472b-4e47-9910-af0bf12fde77 | 2026-07-27 | Warnings, Adverse reactions | 5QZO15J2Z8 |
| Pepcid Complete | FAMOTIDINE, CALCIUM CARBONATE, AND MAGNESIUM HYDROXIDE | Kenvue Brands LLC | a2ef8424-7d80-42b0-a01e-f378f629b2b6 | 2026-07-24 | Warnings | 5QZO15J2Z8 |
| Ibuprofen | IBUPROFEN | REMEDYREPACK INC. | a7756b22-73cf-4262-aa8e-0577ddecd03b | 2026-07-24 | Boxed warning, Warnings, Adverse reactions | 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 |
| Droptics Dry Eye Relief | CARBOXYMETHYLCELLULOSE SODIUM,GLYCERIN,POLYSORBATE 80 | Droptics LLC | 29d7614b-f4b7-48e2-97c5-d1bff27731d2 | 2026-07-22 | Warnings | PDC6A3C0OX |
| Ibuprofen | IBUPROFEN | TWIN MED LLC | f03958f8-aeae-edf0-e053-2a95a90a3e9e | 2026-07-22 | Warnings | WK2XYI10QM |
| GOOD NEIGHBOR PHARMACY ARTIFICAL TEARS LUBRICANT EYE DROPS | POLYVINYL ALCOHOL, POVIDONE | AmerisourceBergen | ce6852a8-c5e6-403d-a7b4-a2e85d1ebb1f | 2026-07-22 | Warnings | FZ989GH94E |
| COMPLETE ACID REDUCER | FAMOTIDINE, CALCIUM CARBONATE AND MAGNESIUM HYDROXIDE | CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED | 962ced24-0fb3-4aba-b32e-2e6fa1c1c5d7 | 2026-07-22 | Warnings | 5QZO15J2Z8 |
| 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 | WK2XYI10QM |
| Ibuprofen | IBUPROFEN | PD-Rx Pharmaceuticals, Inc. | b81c6495-8b30-41ef-8a0f-4cbfd87f1eb4 | 2026-07-21 | Boxed warning, Warnings, Adverse reactions | WK2XYI10QM |
| Ibuprofen | IBUPROFEN | PD-Rx Pharmaceuticals, Inc. | 0cb73c19-a7cb-4ad9-9aa5-c24afb80d6d8 | 2026-07-20 | Boxed warning, Warnings, Adverse reactions | 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 | WK2XYI10QM |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.