NDC11 66343011760
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 |
|---|---|
| 66343-0117-60 | 66343-0117 |
| 66343-117-60 | 66343-117 |
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 |
|---|---|---|---|---|---|---|
| Neurovita | AMBRA GRISEA, CEREBRUM, CINCHONA, CUPRUM ACET, MELISSA, PHOSPHORUS | RUBIMED AG | 333b9c94-8457-47b0-8089-c21268b85b92 | 2026-02-05 | Warnings | 66343-117-60 66343-117 66343011760 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.