NDC 42799-952-01 - Pantoprazole 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
- 42799-952
- Requested NDC
- 42799-952-01
- Package NDCs from labels
- 42799-952-01, 42799-952-30
- Manufacturer
- Edenbridge Pharmaceuticals LLC.
- Effective date
- 2026-07-22
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Pantoprazole Sodium - Edenbridge Pharmaceuticals LLC. | Edenbridge Pharmaceuticals LLC. | 2026-07-22 | Human Prescription Drug Label |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 42799-952-01 | Pantoprazole Sodium | 1 in 1 PACKET | GRANULE, DELAYED RELEASE | 1 | 4 | |
| 42799-952-30 | Pantoprazole Sodium | 30 in 1 CARTON | GRANULE, DELAYED RELEASE | 30 | 4 |
DailyMed Dashboard NDC Coverage#
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 42799-952-01 | EA - Each | 42799-952 | a200ed55-600b-4525-9427-aa61691d54c4 | 1 | 2023-09-05 |
| 42799-952-30 | EA - Each | 42799-952 | 7025722f-4af1-4160-b76d-87fe576e61fd | 1 | 2023-09-05 |
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 |
|---|---|---|---|---|---|---|
| Fertility Drops 2174 | FERTILITY DROPS | Professional Complementary Health Formulas | 78985992-bb47-4045-82f3-a6094e48d50a | 2026-01-08 | Warnings | 45P3261C7T |
| PANTOPRAZOLE SODIUM | PANTOPRAZOLE | Northwind Health Company, LLC | da67e1c0-9947-957d-e053-2a95a90ad96d | 2026-01-01 | Warnings, Adverse reactions | 6871619Q5X |
| Pantoprazole Sodium | PANTOPRAZOLE SODIUM | Northwind Health Company, LLC | f2a1af50-a051-3e55-e053-2a95a90a9184 | 2026-01-01 | Warnings, Adverse reactions | 6871619Q5X |
| Pantoprazole Sodium | PANTOPRAZOLE SODIUM | Northwind Health Company, LLC | d9deb251-96d3-5f96-e053-2a95a90a0792 | 2026-01-01 | Warnings, Adverse reactions | 6871619Q5X |
| Pantoprazole Sodium | PANTOPRAZOLE SODIUM | Cardinal Health 107, LLC | 410d5577-e50a-44f3-aaa8-fbf391a0c261 | 2025-12-30 | Warnings, Adverse reactions | 6871619Q5X |
| Pantoprazole Sodium | PANTOPRAZOLE SODIUM | Chartwell RX, LLC | 42a969c3-1144-4151-9cf3-3e9bace6a380 | 2025-12-22 | Warnings, Adverse reactions | 6871619Q5X |
| Protonix I.V. | PANTOPRAZOLE SODIUM | Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc. | 51e4144a-489e-436c-609a-39305f8f56ba | 2025-12-22 | Warnings, Adverse reactions | 6871619Q5X |
| Protonix I.V. | PANTOPRAZOLE SODIUM | Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc. | f39b3e7d-39d2-4c8a-9974-4ab885241880 | 2025-12-22 | Warnings, Adverse reactions | 6871619Q5X |
| Irritable Bowel Syndrome Therapy | ASAFETIDA - BISMUTH SUBNITRATE - BRYONIA ALBA ROOT - ACTIVATED CHARCOAL - LYCOPODIUM CLAVATUM SPORE - SODIUM CARBONATE - STRYCHNOS NUX-VOMICA SEED - VERATRUM ALBUM ROOT - | TRP Company | 04149220-c7ce-4312-9630-f93d6def3aaa | 2025-12-15 | Warnings | 45P3261C7T |
| PANTOPRAZOLE SODIUM | PANTOPRAZOLE | QPharma Inc | b4a94a37-47c1-4dd9-9e4d-5b4a03480aa6 | 2025-12-04 | Warnings, Adverse reactions | 6871619Q5X |
| Pantoprazole Sodium | PANTOPRAZOLE SODIUM | AvPAK | b9fa8381-b75e-b1cd-e053-2a95a90a9883 | 2025-12-03 | Warnings, Adverse reactions | 6871619Q5X |
| Pantoprazole Sodium | PANTOPRAZOLE SODIUM | QPharma Inc | fbd035d0-529c-6033-e053-6294a90abf07 | 2025-12-02 | Warnings, Adverse reactions | 6871619Q5X |
| Pantoprazole sodium | PANTOPRAZOLE SODIUM | Ajanta Pharma USA Inc. | 90963a38-f629-45a4-bddd-9e13a55fe0f7 | 2025-11-26 | Warnings, Adverse reactions | 763306 6871619Q5X |
| Pantoprazole Sodium | PANTOPRAZOLE | PHOENIX RX LLC | 440b9ae8-2fb8-5d35-e063-6294a90a82b6 | 2025-11-20 | Warnings, Adverse reactions | 6871619Q5X |
| Pantoprazole | PANTOPRAZOLE | PHOENIX RX LLC | 43fc6326-cfe6-7d1c-e063-6394a90abc24 | 2025-11-19 | Warnings, Adverse reactions | 6871619Q5X |
| Pantoprazole Sodium | PANTOPRAZOLE SODIUM | Cardinal Health 107, LLC | 4ba4c797-3f97-4d85-971e-7b17bdf89221 | 2025-11-06 | Warnings, Adverse reactions | 6871619Q5X |
| Pantoprazole | PANTOPRAZOLE | Advanced Rx of Tennessee, LLC | 4136d983-75fa-9604-e063-6294a90aaac6 | 2025-10-15 | Warnings, Adverse reactions | 6871619Q5X |
| Pantoprazole Sodium | PANTOPRAZOLE SODIUM | Cardinal Health 107, LLC | 362229c5-7b28-4563-aa62-d97d06005480 | 2025-10-13 | Warnings, Adverse reactions | 6871619Q5X |
| PANTOPRAZOLE SODIUM I.V. | PANTOPRAZOLE SODIUM | Piramal Critical Care | 0696b10c-972b-9dcf-e063-6294a90a1034 | 2025-10-07 | Warnings, Adverse reactions | 6871619Q5X |
| Pantoprazole Sodium | PANTOPRAZOLE SODIUM | PD-Rx Pharmaceuticals, Inc. | b422c5eb-9a6d-4f8c-863d-ca515ec780c2 | 2025-10-02 | Warnings, Adverse reactions | 6871619Q5X |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.