NDC 80425-0134-01 - Rabeprazole Sodium DR
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
- 80425-0134
- Requested NDC
- 80425-0134-01
- Package NDCs from labels
- 80425-0134-2, 80425-0134-1, 80425-0134-3, 80425-0134-4, 80425-0134-01
- Manufacturer
- Advanced Rx Pharmacy of Tennessee, LLC
- Effective date
- 2026-03-26
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Rabeprazole Sodium DR - Advanced Rx Pharmacy of Tennessee, LLC | Advanced Rx Pharmacy of Tennessee, LLC | 2026-03-26 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 80425-0134-1 | Rabeprazole SodiumDR | 30 in 1 BOTTLE | TABLET, DELAYED RELEASE | 30 | 9 | |
| 80425-0134-2 | Rabeprazole SodiumDR | 60 in 1 BOTTLE | TABLET, DELAYED RELEASE | 60 | 9 | |
| 80425-0134-3 | Rabeprazole SodiumDR | 90 in 1 BOTTLE | TABLET, DELAYED RELEASE | 90 | 9 | |
| 80425-0134-4 | Rabeprazole SodiumDR | 6 in 1 BOTTLE | TABLET, DELAYED RELEASE | 6 | 9 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 80425-0134 | RABEPRAZOLE SODIUM DR (RABEPRAZOLE SODIUM) TABLET, DELAYED RELEASE [ADVANCED RX PHARMACY OF TENNESSEE, LLC] | 8 | Current NDC, Legacy NDC, 4 package rows | 20250101_bdad0b58-495e-2352-e053-2a95a90a3198.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 80425-0134-1 | EA - Each | 80425-0134 | 46a95f21-cdc8-4907-b4ba-c646a92204d7 | 1 | 2023-03-13 |
| 80425-0134-2 | EA - Each | 80425-0134 | e46ac006-dd6d-4ebe-b3e2-eb28e82a0584 | 1 | 2023-03-13 |
| 80425-0134-3 | EA - Each | 80425-0134 | 73fa05d4-1265-40c0-85db-99022dc60885 | 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 |
|---|---|---|---|---|---|---|
| RABEPRAZOLE SODIUM | RABEPRAZOLE SODIUM | Advanced Rx of Tennessee, LLC | 26f8c3bc-4402-e92c-e063-6294a90a9ad7 | 2024-11-15 | Warnings, Adverse reactions | 854868 3L36P16U4R |
| Rabeprazole Sodium | RABEPRAZOLE SODIUM | Bryant Ranch Prepack | 9ea2552c-873c-4ab2-84b0-dd54e84e4eee | 2024-08-21 | Warnings, Adverse reactions | ANDA208644 854868 3L36P16U4R |
| Rabeprazole Sodium | RABEPRAZOLE SODIUM | Bryant Ranch Prepack | 8d8c1a72-b4c4-4699-b9c3-3a39a9df44f2 | 2024-07-16 | Warnings, Adverse reactions | ANDA208644 854868 3L36P16U4R |
| Rabeprazole Sodium | RABEPRAZOLE SODIUM | Proficient Rx LP | 14412af6-e99c-4264-bc34-28a6f139f252 | 2024-07-01 | Warnings, Adverse reactions | 854868 3L36P16U4R |
| Rabeprazole Sodium | RABEPRAZOLE SODIUM | Bryant Ranch Prepack | b35f376a-f2a4-4eb9-80ac-9c20ceb2f0bf | 2024-05-20 | Warnings, Adverse reactions | 854868 3L36P16U4R |
| Rabeprazole Sodium | RABEPRAZOLE SODIUM | Golden State Medical Supply, Inc. | 87231460-8b1e-b995-e053-2a91aa0a6c43 | 2024-04-16 | Warnings, Adverse reactions | 854868 3L36P16U4R |
| Rabeprazole Sodium | RABEPRAZOLE SODIUM | Aurobindo Pharma Limited | d11c3211-b4d4-4893-8c1c-b8fb6d0a0b89 | 2024-02-28 | Warnings, Adverse reactions | 854868 3L36P16U4R |
| RABEPRAZOLE SODIUM | RABEPRAZOLE SODIUM | A-S Medication Solutions | bafff1ac-02fb-4726-b2d7-6e099ae981cb | 2023-12-11 | Warnings, Adverse reactions | 854868 3L36P16U4R |
| Rabeprazole Sodium | RABEPRAZOLE SODIUM | Bryant Ranch Prepack | e6350638-99b0-474d-be75-ae2a3e1af2cf | 2023-12-04 | Warnings, Adverse reactions | 854868 3L36P16U4R |
| Rabeprazole Sodium | RABEPRAZOLE | Amneal Pharmaceuticals LLC | 951caefe-6e18-48ff-9567-beb545b09c25 | 2023-11-30 | Warnings, Adverse reactions | 854868 3L36P16U4R |
| Rabeprazole Sodium | RABEPRAZOLE SODIUM | Lannett Company, Inc. | 7f7d68f0-972b-4315-b712-0bb8a84c85cc | 2023-07-31 | Warnings, Adverse reactions | 854868 3L36P16U4R |
| Rabeprazole Sodium | RABEPRAZOLE SODIUM | A-S Medication Solutions | 4ded337a-31b8-47c3-b5ab-33a785afb7d8 | 2023-02-06 | Warnings, Adverse reactions | ANDA208644 854868 3L36P16U4R |
| RABEPRAZOLE SODIUM | RABEPRAZOLE SODIUM | Asclemed USA, Inc. | 9881dbb2-1ce2-4737-989f-b26720791ca5 | 2022-07-07 | Warnings, Adverse reactions | 854868 3L36P16U4R |
| RABEPRAZOLE SODIUM | RABEPRAZOLE SODIUM | Proficient Rx LP | 0f5eb1b4-ad4b-4782-8d3d-cd33f9c5be7d | 2022-04-01 | Warnings, Adverse reactions | 854868 3L36P16U4R |
| Rabeprazole sodium | RABEPRAZOLE SODIUM | Proficient Rx LP | d1444508-fe40-4f68-8350-52f13399e38a | 2021-01-01 | Warnings, Adverse reactions | 854868 3L36P16U4R |
| Rabeprazole Sodium | RABEPRAZOLE SODIUM | Asclemed USA, Inc. | 12eaf996-db61-41d6-82e1-fa6196435603 | 2020-06-26 | Warnings, Adverse reactions | 854868 3L36P16U4R |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.