NDC11 61649073201
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 |
|---|---|
| 61649-0732-01 | 61649-0732 |
| 61649-0732-1 | 61649-0732 |
| 61649-732-01 | 61649-732 |
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 | d33e3778-ba1d-4560-bafa-74f7ab88c6b5 | 2025-01-20 | Warnings | 61649-732-01 61649-732 61649073201 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.