NDC11 68083011301
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 |
|---|---|
| 68083-0113-01 | 68083-0113 |
| 68083-0113-1 | 68083-0113 |
| 68083-113-01 | 68083-113 |
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 |
|---|---|---|---|---|---|---|
| Ondansetron | ONDANSETRON | Gland Pharma Limited | 3efa5604-96c3-42a0-8e99-b3de4a66aa92 | 2025-07-31 | Warnings, Adverse reactions | 68083-113-01 68083-113 68083011301 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.