NDC11 60687084101
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 |
|---|---|
| 60687-0841-01 | 60687-0841 |
| 60687-0841-1 | 60687-0841 |
| 60687-841-01 | 60687-841 |
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 |
|---|---|---|---|---|---|---|
| Extended Phenytoin Sodium | PHENYTOIN SODIUM | American Health Packaging | 5b64cb11-673a-41ec-9b2a-1e194ae5eb0c | 2025-02-06 | Warnings, Adverse reactions | 60687-841-01 60687-841 60687084101 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.