NDC11 68462031740
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 |
|---|---|
| 68462-0317-40 | 68462-0317 |
| 68462-317-40 | 68462-317 |
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 | GLENMARK PHARMACEUTICALS INC., USA | 99cf8b69-4c23-4886-80e9-b23e348b5bd7 | 2026-02-27 | Warnings, Adverse reactions | 68462-317-40 68462-317 68462031740 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.