NDC11 51660020005
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 |
|---|---|
| 51660-0200-05 | 51660-0200 |
| 51660-0200-5 | 51660-0200 |
| 51660-200-05 | 51660-200 |
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 |
|---|---|---|---|---|---|---|
| Ezetimibe | EZETIMIBE | Ohm Laboratories Inc. | 5b3842f6-c80a-47b8-8a82-b69e465b05f7 | 2024-03-05 | Warnings, Adverse reactions | 51660-200-05 51660-200 51660020005 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.