NDC11 68001067008
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 |
|---|---|
| 68001-0670-08 | 68001-0670 |
| 68001-0670-8 | 68001-0670 |
| 68001-670-08 | 68001-670 |
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 |
|---|---|---|---|---|---|---|
| Fluoxetine | FLUOXETINE | BluePoint Laboratories | daf33244-1348-4c34-b44c-9e35d5c48a3e | 2026-03-25 | Boxed warning, Warnings, Adverse reactions | 68001-670-08 68001-670 68001067008 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.