NDC11 61649073001
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 |
|---|---|
| 61649-0730-01 | 61649-0730 |
| 61649-0730-1 | 61649-0730 |
| 61649-730-01 | 61649-730 |
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 |
|---|---|---|---|---|---|---|
| BIO SPECTRA ATTITUDE | SODIUM FLUORIDE | 9055-7588 Quebec Inc. DBA Attitude | e3bb60f8-2a06-42d6-a182-8c31bb982a2a | 2024-03-01 | Warnings | 61649-730-01 61649-730 61649073001 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.