NDC11 48951510801
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 |
|---|---|
| 48951-5108-01 | 48951-5108 |
| 48951-5108-1 | 48951-5108 |
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 |
|---|---|---|---|---|---|---|
| Helleborus e pl. tota 12 | HELLEBORUS E PL. TOTA 12 | Uriel Pharmacy Inc. | 6ccb8d0f-6c0b-26ae-e053-2991aa0abeb8 | 2025-01-22 | Warnings | 48951-5108-1 48951-5108 48951510801 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.