NDC11 36800009705
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 |
|---|---|
| 36800-0097-05 | 36800-0097 |
| 36800-0097-5 | 36800-0097 |
| 36800-097-05 | 36800-097 |
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 |
|---|---|---|---|---|---|---|
| Eye Itch Relief | KETOTIFEN FUMARATE | TOPCO ASSOCIATES LLC | b723daa3-6c6f-4a96-a15d-0d5866f28ca4 | 2023-12-08 | Warnings | 36800-097-05 36800-097 36800009705 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.