NDC11 68682010301
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 |
|---|---|
| 68682-0103-01 | 68682-0103 |
| 68682-0103-1 | 68682-0103 |
| 68682-103-01 | 68682-103 |
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 | DICLOFENAC SODIUM | Oceanside Pharmaceuticals | c48113e0-9f1e-4086-b18f-3204c0d2a689 | 2025-03-13 | Boxed warning, Warnings, Adverse reactions | 68682-103-01 68682-103 68682010301 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.