NDC11 00299593545
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 |
|---|---|
| 00299-5935-45 | 00299-5935 |
| 0299-5935-45 | 0299-5935 |
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 |
|---|---|---|---|---|---|---|
| AKLIEF | TRIFAROTENE | Galderma Laboratories, L.P. | 62d910db-85a6-4696-b69b-4bd2f3080cfc | 2024-09-16 | Warnings, Adverse reactions | 0299-5935-45 0299-5935 00299593545 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.