NDC 55111-332-79 - Pantoprazole
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
- 55111-332
- Requested NDC
- 55111-332-79
- Package NDCs from labels
- 55111-332-30, 55111-332-90, 55111-332-01, 55111-332-05, 55111-332-10, 55111-332-79, 55111-332-81, 55111-332-78
- Manufacturer
- Preferred Pharmaceuticals Inc.
- Effective date
- 2026-08-11
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Pantoprazole - Preferred Pharmaceuticals Inc. | Preferred Pharmaceuticals Inc. | 2026-08-11 | HUMAN PRESCRIPTION DRUG LABEL |
| Pantoprazole - Coupler LLC | Coupler LLC | 2026-06-19 | HUMAN PRESCRIPTION DRUG LABEL |
| Pantoprazole - St. Mary's Medical Park Pharmacy | St. Mary's Medical Park Pharmacy | 2026-06-17 | HUMAN PRESCRIPTION DRUG LABEL |
| Pantoprazole - PHOENIX RX LLC | PHOENIX RX LLC | 2025-11-19 | HUMAN PRESCRIPTION DRUG LABEL |
| Pantoprazole - Advanced Rx of Tennessee, LLC | Advanced Rx of Tennessee, LLC | 2025-10-15 | HUMAN PRESCRIPTION DRUG LABEL |
| Pantoprazole - REMEDYREPACK INC. | REMEDYREPACK INC. | 2024-05-03 | HUMAN PRESCRIPTION DRUG LABEL |
| Pantoprazole - NuCare Pharmaceuticals,Inc. | NuCare Pharmaceuticals,Inc. | 2023-10-18 | HUMAN PRESCRIPTION DRUG LABEL |
| Pantoprazole - Dr.Reddy's Laboratories Limited | Dr.Reddy's Laboratories Limited | 2023-08-30 | HUMAN PRESCRIPTION DRUG LABEL |
| Pantoprazole - State of Florida DOH Central Pharmacy | State of Florida DOH Central Pharmacy | 2015-01-17 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 55111-332-01 | Pantoprazole | 100 in 1 BOTTLE | TABLET, DELAYED RELEASE | 100 | 21 | |
| 55111-332-05 | Pantoprazole | 500 in 1 BOTTLE | TABLET, DELAYED RELEASE | 500 | 21 | |
| 55111-332-10 | Pantoprazole | 1000 in 1 BOTTLE | TABLET, DELAYED RELEASE | 1000 | 21 | |
| 55111-332-30 | Pantoprazole | 30 in 1 BOTTLE | TABLET, DELAYED RELEASE | 30 | 21 | |
| 55111-332-78 | Pantoprazole | 10 in 1 CARTON | TABLET, DELAYED RELEASE | 10 | 21 | |
| 55111-332-79 | Pantoprazole | 10 in 1 BLISTER PACK | TABLET, DELAYED RELEASE | 10 | 21 | |
| 55111-332-81 | Pantoprazole | 3 in 1 CARTON | TABLET, DELAYED RELEASE | 3 | 21 | |
| 55111-332-90 | Pantoprazole | 90 in 1 BOTTLE | TABLET, DELAYED RELEASE | 90 | 21 |
DailyMed Dashboard NDC Coverage#
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 55111-332-90 | EA - Each | 55111-332 | 86894b47-af09-462c-8565-168152e25106 | 1 | 2012-07-24 |
DailyMed Socrata Ingredients#
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.