NDC11 68987001315
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 |
|---|---|
| 68987-0013-15 | 68987-0013 |
| 68987-013-15 | 68987-013 |
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 |
|---|---|---|---|---|---|---|
| PureLife APF | SODIUM FLUORIDE | PureLife Dental | c8262117-43e6-4771-93ac-618e0f2c8c41 | 2022-01-19 | Warnings | 68987-013-15 68987-013 68987001315 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.