NDC11 71205069200
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 |
|---|---|
| 71205-0692-0 | 71205-0692 |
| 71205-0692-00 | 71205-0692 |
| 71205-692-00 | 71205-692 |
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 | Proficient Rx LP | 67e384c6-8476-4aad-b967-241335538d56 | 2022-08-01 | Boxed warning, Warnings, Adverse reactions | 71205-692-00 71205-692 71205069200 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.