NDC11 48951503801
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 |
|---|---|
| 48951-5038-01 | 48951-5038 |
| 48951-5038-1 | 48951-5038 |
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 4 | HELLEBORUS E PL. TOTA 4 | Uriel Pharmacy Inc. | 462c4c00-8469-45d1-9029-2aa48b0f4af9 | 2026-06-16 | Warnings | 48951-5038-1 48951-5038 48951503801 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.