NDC11 69452035113
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 |
|---|---|
| 69452-0351-13 | 69452-0351 |
| 69452-351-13 | 69452-351 |
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 | Bionpharma Inc. | 34221c17-0d8c-4b56-8af3-c74efab4599e | 2024-12-18 | Warnings, Adverse reactions | 69452-351-13 69452-351 69452035113 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.