NDC11 48951140905
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 |
|---|---|
| 48951-1409-05 | 48951-1409 |
| 48951-1409-5 | 48951-1409 |
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 |
|---|---|---|---|---|---|---|
| Argentum 5X | ARGENTUM 5X | Uriel Pharmacy, Inc | 4bd30e47-c039-06e8-e063-6294a90a8c4d | 2026-02-27 | Warnings | 48951-1409-5 48951-1409 48951140905 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.