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 | 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 |
| ACID REDUCER | FAMOTIDINE | CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED | f347f870-1da4-4a77-8c20-63b703d24071 | 2026-08-05 | Warnings | 5QZO15J2Z8 |
| 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 |
| Dye Free Ibuprofen | IBUPROFEN | Walgreen Company | 8944a0e8-2928-4494-915f-d1e0a6d4bf5c | 2026-08-04 | Warnings | WK2XYI10QM |
| ROROBELL WAWA Whitening Tooth | SILICA, HYDROGEN PEROXIDE, TOCOPHERYL ACETATE | ROROBELL | 58336a0d-49dd-ef13-e063-6394a90a38c1 | 2026-08-04 | Warnings | ETJ7Z6XBU4 |
| Ibuprofen | IBUPROFEN | REMEDYREPACK INC. | 560e4e05-21e0-4b2a-ab2f-872b5dbb3901 | 2026-08-04 | Boxed warning, Warnings, Adverse reactions | WK2XYI10QM |
| CVS Glycerin | GLYCERIN SUPPOISITORY | CVS Pharmacy, Inc | ca6d13db-60e8-4fcc-b7b3-3eb280b8c435 | 2026-08-04 | Warnings | PDC6A3C0OX |
| Silicea 6X | SILICON DIOXIDE | Hyland's Inc. | db4be3c1-aa7e-24a2-e053-2a95a90a0c66 | 2026-08-04 | Warnings | ETJ7Z6XBU4 |
| Ibuprofen | IBUPROFEN | Chain Drug Marketing Association, Inc. | 733d0b21-c177-4c60-9243-2f1e7cb5854a | 2026-08-04 | Warnings | WK2XYI10QM |
| Ibuprofen | IBUPROFEN | Pioneer Life Sciences, LLC | 8abd74a4-ad33-4c10-b677-acb469f815e6 | 2026-08-03 | Warnings | WK2XYI10QM |
| Ibuprofen | IBUPROFEN | Pioneer Life Sciences, LLC | 291602fa-8ebe-4200-bba7-9798c90f8a50 | 2026-08-03 | Warnings | WK2XYI10QM |
| Ibuprofen | IBUPROFEN | NUVICARE LLC | b063d2dc-d579-46e7-8cfc-1596c803c7f9 | 2026-08-03 | Warnings | WK2XYI10QM |
| Ibuprofen | IBUPROFEN | NUVICARE LLC | 7905edc1-2a45-4adc-a7bc-42b1ddb6ba59 | 2026-08-03 | Warnings | WK2XYI10QM |
| Ibuprofen and famotidine | IBUPROFEN AND FAMOTIDINE | Doc Rx | 9f5de6af-e555-4efd-a3ed-b72c34c051b6 | 2026-08-01 | Boxed warning, Warnings, Adverse reactions | 1100066 WK2XYI10QM 5QZO15J2Z8 |
| Ibuprofen and Pseudoephedrine Hydrochloride | IBUPROFEN AND PSEUDOEPHEDRINE HYDROCHLORIDE | Rite-Aid | 483c3bb7-529e-4684-80e1-6646b050988e | 2026-07-31 | Warnings | WK2XYI10QM |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.