NDC11 48951930401
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 |
|---|---|
| 48951-9304-01 | 48951-9304 |
| 48951-9304-1 | 48951-9304 |
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 |
|---|---|---|---|---|---|---|
| Viscum Abietis 10 | VISCUM ABIETIS 10 | Uriel Pharmacy Inc. | 70c0766a-3965-49bd-9d9e-e87a299b18ba | 2025-11-26 | Warnings | 48951-9304-1 48951-9304 48951930401 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.