NDC11 48951131801
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 |
|---|---|
| 48951-1318-01 | 48951-1318 |
| 48951-1318-1 | 48951-1318 |
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 |
|---|---|---|---|---|---|---|
| Aurum 21X | AURUM 21X | Uriel Pharmacy Inc. | 93f243c0-b963-9ea0-e053-2995a90aa852 | 2026-01-16 | Warnings | 48951-1318-1 48951-1318 48951131801 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.