NDC11 51672207304
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 |
|---|---|
| 51672-2073-04 | 51672-2073 |
| 51672-2073-4 | 51672-2073 |
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 |
|---|---|---|---|---|---|---|
| Childrens Loratadine | LORATADINE | Sun Pharmaceutical Industries, Inc. | 78e11f1c-c8a4-4b2a-b7dc-ae1b2dea26d0 | 2026-04-08 | Warnings | 51672-2073-4 51672-2073 51672207304 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.