NDC11 68001062686
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 |
|---|---|
| 68001-0626-86 | 68001-0626 |
| 68001-626-86 | 68001-626 |
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 |
|---|---|---|---|---|---|---|
| Fulvestrant | FULVESTRANT | BluePoint Laboratories. | 57352662-d2fa-4dce-828f-4c51e46e0b4d | 2025-07-25 | Warnings, Adverse reactions | 68001-626-86 68001-626 68001062686 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.