NDC11 68999073045
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 |
|---|---|
| 68999-0730-45 | 68999-0730 |
| 68999-730-45 | 68999-730 |
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 |
|---|---|---|---|---|---|---|
| Fluoxetine | FLUOXETINE | Chartwell Governmental & Specialty RX, LLC | d34362ed-e821-4c55-9f8c-3dfb772b1b2a | 2026-02-11 | Boxed warning, Warnings, Adverse reactions | 68999-730-45 68999-730 68999073045 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.