NDC11 48951313805
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 |
|---|---|
| 48951-3138-05 | 48951-3138 |
| 48951-3138-5 | 48951-3138 |
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 |
|---|---|---|---|---|---|---|
| Cuprum 5 | CUPRUM 5 | Uriel Pharmacy Inc. | 6c6ffab3-985a-49f2-9de5-a0736d5d85cf | 2025-06-27 | Warnings | 48951-3138-5 48951-3138 48951313805 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.