NDC11 68001031700
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 |
|---|---|
| 68001-0317-0 | 68001-0317 |
| 68001-0317-00 | 68001-0317 |
| 68001-317-00 | 68001-317 |
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 |
|---|---|---|---|---|---|---|
| Nadolol | NADOLOL | BluePoint Laboratories | 0a2acdc0-aab6-462e-a377-67a0f3d55ec6 | 2024-05-28 | Boxed warning, Warnings, Adverse reactions | 68001-317-00 68001-317 68001031700 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.