NDC11 71205090800
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 |
|---|---|
| 71205-0908-0 | 71205-0908 |
| 71205-0908-00 | 71205-0908 |
| 71205-908-00 | 71205-908 |
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 | Proficient Rx LP | 46d12bd0-ec7d-4e2c-aeed-b8aa88e6dc5c | 2022-03-01 | Warnings, Adverse reactions | 71205-908-00 71205-908 71205090800 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.