NDC11 67751015301
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 |
|---|---|
| 67751-0153-01 | 67751-0153 |
| 67751-0153-1 | 67751-0153 |
| 67751-153-01 | 67751-153 |
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 |
|---|---|---|---|---|---|---|
| Claritin | LORATADINE | Navajo Manufacturing Company | 60a5dc14-3f74-8414-e053-2991aa0ad34a | 2023-03-01 | Warnings | 67751-153 |
| Claritin | LORATADINE | Navajo Manufacturing Company Inc. | 219ab9c4-d0c4-4256-ab64-66d0260886bd | 2023-03-01 | Warnings | 67751-153-01 67751-153 67751015301 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.