NDC11 68682024101
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 |
|---|---|
| 68682-0241-01 | 68682-0241 |
| 68682-0241-1 | 68682-0241 |
| 68682-241-01 | 68682-241 |
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 |
|---|---|---|---|---|---|---|
| Azathioprine | AZATHIOPRINE | Oceanside Pharmaceuticals | d72ede2c-1a9b-4717-80a7-b76a6a499936 | 2025-09-22 | Boxed warning, Warnings, Adverse reactions | 68682-241-01 68682-241 68682024101 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.