NDC11 51991052601
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 |
|---|---|
| 51991-0526-01 | 51991-0526 |
| 51991-0526-1 | 51991-0526 |
| 51991-526-01 | 51991-526 |
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 | Breckenridge Pharmaceutical, Inc. | c3832113-f517-4b4e-bf9c-31fce1a638e1 | 2023-12-22 | Warnings, Adverse reactions | 51991-526-01 51991-526 51991052601 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.