NDC11 68001023106
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 |
|---|---|
| 68001-0231-06 | 68001-0231 |
| 68001-0231-6 | 68001-0231 |
| 68001-231-06 | 68001-231 |
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 |
|---|---|---|---|---|---|---|
| Diclofenac Sodium and Misoprostol | DICLOFENAC SODIUM AND MISOPROSTOL | BluePoint Laboratories | 9a22cb4b-e49a-4bd7-b235-47405c302658 | 2025-09-11 | Boxed warning, Warnings, Adverse reactions | 68001-231-06 68001-231 68001023106 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.