NDC11 60687090921
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 |
|---|---|
| 60687-0909-21 | 60687-0909 |
| 60687-909-21 | 60687-909 |
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 | American Health Packaging | 4ee1b667-0cf6-46e4-a740-4fc27904d577 | 2026-03-06 | Warnings, Adverse reactions | 60687-909-21 60687-909 60687090921 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.