NDC11 55259000101
This exact 11-digit normalized identifier can correspond to more than one FDA hyphenation. FDA.report preserves the exact identifier and exposes every structurally valid candidate without guessing.
Possible FDA NDC forms#
| Package NDC | Product root |
|---|---|
| 55259-0001-01 | 55259-0001 |
| 55259-0001-1 | 55259-0001 |
| 55259-001-01 | 55259-001 |
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 |
|---|---|---|---|---|---|---|
| 7030 Calcium Gold | CALCIUM | Apexel Co., Ltd | bdc7c088-83e3-20ce-e053-2995a90abd2f | 2024-02-20 | Warnings | 55259-0001-1 55259-0001 55259000101 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.