NDC11 80425005601
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 |
|---|---|
| 80425-0056-01 | 80425-0056 |
| 80425-0056-1 | 80425-0056 |
| 80425-056-01 | 80425-056 |
Observed NDC auxiliary status history#
This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
| Captured / source date | Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Archive | Snapshot | Source SHA-256 |
|---|---|---|---|---|---|---|---|---|---|---|
| 2021-12-27 23:28 UTC · source 2021-12-27 | excluded package | package | 80425-0056 | 80425-0056-1 | E | Excluded after deficient or non-compliant submission was not corrected | excluded / ndc_excluded.zip | 8dfbde2a14a4… | c9ff85d89658… |
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 DR | DICLOFENAC | Advanced Rx of Tennessee, LLC | af8a30fb-ead8-7e29-e053-2a95a90a040f | 2024-12-31 | Boxed warning, Warnings, Adverse reactions | 80425-0056-1 80425-0056 80425005601 |