NDC11 00023927705
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 |
|---|---|
| 00023-9277-05 | 00023-9277 |
| 00023-9277-5 | 00023-9277 |
| 0023-9277-05 | 0023-9277 |
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 |
|---|---|---|---|---|---|---|
| ACULAR LS | KETOROLAC TROMETHAMINE | Allergan, Inc. | 4fad0873-f79c-4f07-9fac-5060be6b38fe | 2024-06-21 | Warnings, Adverse reactions | 0023-9277-05 0023-9277 00023927705 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.