NDC11 00591438579
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 |
|---|---|
| 00591-4385-79 | 00591-4385 |
| 0591-4385-79 | 0591-4385 |
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 |
|---|---|---|---|---|---|---|
| Fosaprepitant | FOSAPREPITANT | Actavis Pharma, Inc. | 9dbd4c29-d894-4839-9b22-a2f65c8c8ad1 | 2022-06-30 | Warnings, Adverse reactions | 0591-4385-79 0591-4385 00591438579 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.