NDC11 63323071059
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 |
|---|---|
| 63323-0710-59 | 63323-0710 |
| 63323-710-59 | 63323-710 |
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 |
|---|---|---|---|---|---|---|
| Leucovorin Calcium | LEUCOVORIN CALCIUM | Fresenius Kabi USA, LLC | ab691d4e-e0d1-4ba1-9c7a-1cdcfcc3c17c | 2024-10-14 | Warnings, Adverse reactions | 63323-710-59 63323-710 63323071059 |
| Leucovorin Calcium | LEUCOVORIN CALCIUM | Fresenius Kabi USA, LLC | e3b957dc-a542-4f69-b8a0-7df401ee706f | 2022-03-03 | Warnings, Adverse reactions | 63323-710 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.