NDC11 48951930101
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 |
|---|---|
| 48951-9301-01 | 48951-9301 |
| 48951-9301-1 | 48951-9301 |
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 1 | VISCUM ABIETIS 1 | Uriel Pharmacy Inc. | c9020643-a718-4709-aefd-ab02af6ec551 | 2026-01-16 | Warnings | 48951-9301-1 48951-9301 48951930101 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.