NDC11 24208060190
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 |
|---|---|
| 24208-0601-90 | 24208-0601 |
| 24208-601-90 | 24208-601 |
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 |
|---|---|---|---|---|---|---|
| Alaway | KETOTIFEN FUMARATE | Bausch & Lomb Incorporated | e4c310b5-1dba-4ddc-bc90-b27ebc765871 | 2022-05-01 | Warnings | 24208-601-90 24208-601 24208060190 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.