NDC11 51655036426
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 |
|---|---|
| 51655-0364-26 | 51655-0364 |
| 51655-364-26 | 51655-364 |
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 |
|---|---|---|---|---|---|---|
| Terbinafine Hydrochloride | TERBINAFINE HYDROCHLORIDE | Northwind Health Company, LLC | ab6f50a5-87ce-0819-e053-2a95a90a22b7 | 2026-01-01 | Warnings, Adverse reactions | 51655-364-26 51655-364 51655036426 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.