NDC11 17089037018
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 |
|---|---|
| 17089-0370-18 | 17089-0370 |
| 17089-370-18 | 17089-370 |
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 |
|---|---|---|---|---|---|---|
| GUNA-BDNF | BRAIN-DERIVED NEUROTROPHIC FACTOR | Guna spa | a5b5bd86-691b-44d8-b412-07022fb43e54 | 2026-06-11 | Warnings | 17089-370-18 17089-370 17089037018 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.