NDC 67877-443-33 - Rabeprazole Sodium
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
- 67877-443
- Requested NDC
- 67877-443-33
- Package NDCs from labels
- 67877-443-30, 67877-443-90, 67877-443-33, 67877-443-38
- Manufacturer
- REMEDYREPACK INC.
- Effective date
- 2026-09-28
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Rabeprazole Sodium - REMEDYREPACK INC. | REMEDYREPACK INC. | 2026-09-28 | HUMAN PRESCRIPTION DRUG LABEL |
| Rabeprazole Sodium - Ascend Laboratories, LLC | Alkem Laboratories Limited | Ascend Laboratories, LLC | Alkem Laboratories Limited | 2026-08-28 | Human Prescription Drug Label |
| Rabeprazole Sodium - Preferred Pharmaceuticals, Inc. | Preferred Pharmaceuticals, Inc. | 2026-08-25 | HUMAN PRESCRIPTION DRUG LABEL |
| Rabeprazole Sodium - St. Mary's Medical Park Pharmacy | St. Mary's Medical Park Pharmacy | 2026-06-26 | HUMAN PRESCRIPTION DRUG LABEL |
| Rabeprazole Sodium - Proficient Rx LP | Proficient Rx LP | 2026-05-01 | HUMAN PRESCRIPTION DRUG LABEL |
| Rabeprazole Sodium DR - Advanced Rx Pharmacy of Tennessee, LLC | Advanced Rx Pharmacy of Tennessee, LLC | 2026-03-26 | HUMAN PRESCRIPTION DRUG LABEL |
| Rabeprazole Sodium DR - Advanced Rx of Tennessee, LLC | Advanced Rx of Tennessee, LLC | 2026-03-13 | HUMAN PRESCRIPTION DRUG LABEL |
| Rabeprazole Sodium - Asclemed USA, Inc. | ASCLEMED USA INC. DBA ENOVACHEM | Asclemed USA, Inc. | ASCLEMED USA INC. DBA ENOVACHEM | 2026-02-14 | HUMAN PRESCRIPTION DRUG LABEL |
| Rabeprazole Sodium - PHOENIX RX LLC | PHOENIX RX LLC | 2025-07-21 | HUMAN PRESCRIPTION DRUG LABEL |
| RABEPRAZOLE SODIUM - DIRECT RX | DIRECT RX | 2025-01-17 | HUMAN PRESCRIPTION DRUG LABEL |
| Rabeprazole Sodium - Quality Care Products, LLC | Quality Care Products, LLC | 2024-12-18 | Human Prescription Drug Label |
| Rabeprazole Sodium - Bryant Ranch Prepack | Bryant Ranch Prepack | 2024-08-21 | HUMAN PRESCRIPTION DRUG LABEL |
| Rabeprazole Sodium - Bryant Ranch Prepack | Bryant Ranch Prepack | 2024-07-16 | HUMAN PRESCRIPTION DRUG LABEL |
| Rabeprazole Sodium - A-S Medication Solutions | A-S Medication Solutions | 2023-02-06 | Human Prescription Drug Label |
| Rabeprazole Sodium - Medsource Pharmaceuticals | Medsource Pharmaceuticals | 2020-10-25 | HUMAN PRESCRIPTION DRUG LABEL |
| Rabeprazole Sodium - Denton Pharma, Inc. DBA Northwind Pharmaceuticals | Denton Pharma, Inc. DBA Northwind Pharmaceuticals | 2020-08-25 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 67877-443-30 | Rabeprazole Sodium | 30 in 1 BOTTLE | TABLET, DELAYED RELEASE | 30 | 18 | |
| 67877-443-33 | Rabeprazole Sodium | 10 in 1 BLISTER PACK | TABLET, DELAYED RELEASE | 10 | 18 | |
| 67877-443-38 | Rabeprazole Sodium | 100 in 1 CARTON | TABLET, DELAYED RELEASE | 100 | 18 | |
| 67877-443-38 | Rabeprazole Sodium | 1 in 1 POUCH | TABLET, DELAYED RELEASE | 1 | 18 | |
| 67877-443-90 | Rabeprazole Sodium | 90 in 1 BOTTLE | TABLET, DELAYED RELEASE | 90 | 18 |
DailyMed Dashboard NDC Coverage#
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 67877-443-30 | EA - Each | 67877-443 | 7b45b1a3-3c42-42eb-9cb3-66061de665bd | 1 | 2018-11-06 |
| 67877-443-90 | EA - Each | 67877-443 | b88d448e-94bc-47bb-9bfc-15de4e5ef7b6 | 1 | 2018-11-06 |
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.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.