NDC11 68788860903
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 |
|---|---|
| 68788-8609-03 | 68788-8609 |
| 68788-8609-3 | 68788-8609 |
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 |
|---|---|---|---|---|---|---|
| Divalproex Sodium | DIVALPROEX SODIUM | Preferred Pharmaceuticals Inc. | d1d4d790-73d5-4a3b-a786-99f2c9812546 | 2026-04-07 | Boxed warning, Warnings, Adverse reactions | 68788-8609-3 68788-8609 68788860903 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.