NDC11 48951814202
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 |
|---|---|
| 48951-8142-02 | 48951-8142 |
| 48951-8142-2 | 48951-8142 |
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 |
|---|---|---|---|---|---|---|
| Rhus Aconitum | RHUS ACONITUM | Uriel Pharmacy Inc. | a3ef433e-fca5-45dc-a972-b0021e048c53 | 2025-06-27 | Warnings | 48951-8142-2 48951-8142 48951814202 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.