NDC11 71205049242
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 |
|---|---|
| 71205-0492-42 | 71205-0492 |
| 71205-492-42 | 71205-492 |
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 | TERBINAFINE HYDROCHLORIDE | Proficient Rx LP | 50657431-1cd9-42dd-9cfc-57db8713d267 | 2024-04-01 | Warnings, Adverse reactions | 71205-492-42 71205-492 71205049242 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.