NDC11 59011096201
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 |
|---|---|
| 59011-0962-01 | 59011-0962 |
| 59011-0962-1 | 59011-0962 |
| 59011-962-01 | 59011-962 |
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 |
|---|---|---|---|---|---|---|
| Zurnai | NALMEFENE HYDROCHLORIDE | Knoa Pharma LLC | a59a5847-9fe4-4341-a203-be0a5e6d3e36 | 2026-07-31 | Warnings, Adverse reactions | 59011-962-01 59011-962 59011096201 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.