NDC11 49609010101
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 |
|---|---|
| 49609-0101-01 | 49609-0101 |
| 49609-0101-1 | 49609-0101 |
| 49609-101-01 | 49609-101 |
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 |
|---|---|---|---|---|---|---|
| Fludeoxyglucose F 18 | FLUDEOXYGLUCOSE F-18 | SOFIE Co. | 2028be0c-333c-4e0c-be57-099276c725d7 | 2025-11-19 | Warnings, Adverse reactions | 49609-101-01 49609-101 49609010101 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.