NDC11 65162099901
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 |
|---|---|
| 65162-0999-01 | 65162-0999 |
| 65162-0999-1 | 65162-0999 |
| 65162-999-01 | 65162-999 |
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 |
|---|---|---|---|---|---|---|
| Fosphenytoin Sodium | FOSPHENYTOIN SODIUM | Amneal Pharmaceuticals LLC | 87ff8a91-5b37-401c-b75c-dc6efd348761 | 2024-10-25 | Warnings, Adverse reactions | 65162-999-01 65162-999 65162099901 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.