NDC11 11980022805
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 |
|---|---|
| 11980-0228-05 | 11980-0228 |
| 11980-0228-5 | 11980-0228 |
| 11980-228-05 | 11980-228 |
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 |
|---|---|---|---|---|---|---|
| FML FORTE | FLUOROMETHOLONE | Allergan, Inc. | b810b4c3-ac7a-4ba5-85bf-ebfaf3b1dabf | 2025-02-13 | Warnings, Adverse reactions | 11980-228-05 11980-228 11980022805 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.