NDC11 70710168802
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 |
|---|---|
| 70710-1688-02 | 70710-1688 |
| 70710-1688-2 | 70710-1688 |
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 | Zydus Pharmaceuticals USA Inc. | 994edf79-20a5-4e3a-bb35-c4fe3e65acba | 2024-08-20 | Warnings, Adverse reactions | 70710-1688-2 70710-1688 70710168802 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.