NDC11 60290006102
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 |
|---|---|
| 60290-0061-02 | 60290-0061 |
| 60290-0061-2 | 60290-0061 |
| 60290-061-02 | 60290-061 |
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 POTASSIUM | DICLOFENAC POTASSIUM | Umedica Laboratories USA Inc. | 33930285-dd97-415c-9e2a-491bd7b12af9 | 2026-01-30 | Boxed warning, Warnings, Adverse reactions | 60290-061-02 60290-061 60290006102 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.