NDC11 51224020650
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 |
|---|---|
| 51224-0206-50 | 51224-0206 |
| 51224-206-50 | 51224-206 |
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 |
|---|---|---|---|---|---|---|
| Naltrexone Hydrochloride | NALTREXONE HYDROCHLORIDE | TAGI Pharma Inc. | 60276f5c-657a-4b60-bcd0-44234903d7e0 | 2025-11-18 | Warnings, Adverse reactions | 51224-206-50 51224-206 51224020650 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.