NDC11 64764010500
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 |
|---|---|
| 64764-0105-0 | 64764-0105 |
| 64764-0105-00 | 64764-0105 |
| 64764-105-00 | 64764-105 |
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 |
|---|---|---|---|---|---|---|
| Eohilia | BUDESONIDE | TAKEDA PHARMACEUTICALS AMERICA, INC. | 56f2023a-69b2-4470-b4ad-af7ec1be527a | 2025-02-03 | Warnings, Adverse reactions | 64764-105-00 64764-105 64764010500 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.