NDC11 48951841003
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 |
|---|---|
| 48951-8410-03 | 48951-8410 |
| 48951-8410-3 | 48951-8410 |
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 |
|---|---|---|---|---|---|---|
| Stibium 20X | STIBIUM 20X | Uriel Pharmacy Inc. | 13f25caf-51f0-6b2f-e063-6394a90a0920 | 2026-03-30 | Warnings | 48951-8410-3 48951-8410 48951841003 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.