NDC11 00074050101
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 |
|---|---|
| 00074-0501-01 | 00074-0501 |
| 00074-0501-1 | 00074-0501 |
| 00074-501-01 | 00074-501 |
| 0074-0501-01 | 0074-0501 |
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 |
|---|---|---|---|---|---|---|
| Vyalev | FOSCARBIDOPA/FOSLEVODOPA | AbbVie Inc. | 28e806e4-951c-40a9-9f0c-d0929caf054c | 2026-03-19 | Warnings, Adverse reactions | 0074-0501-01 0074-0501 00074050101 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.