NDC11 51660012306
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 |
|---|---|
| 51660-0123-06 | 51660-0123 |
| 51660-0123-6 | 51660-0123 |
| 51660-123-06 | 51660-123 |
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 |
|---|---|---|---|---|---|---|
| Loperamide Hydrochloride | LOPERAMIDE HYDROCHLORIDE | Ohm Laboratories Inc. | c26c15a1-3a8a-4562-8c5e-ebbc8b81e0c6 | 2024-01-11 | Warnings | 51660-123-06 51660-123 51660012306 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.