NDC11 70860021141
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 |
|---|---|
| 70860-0211-41 | 70860-0211 |
| 70860-211-41 | 70860-211 |
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 | Athenex Pharmaceutical Division, LLC. | 8ed06e0e-c17b-4c71-8d03-888bcde4a638 | 2025-01-28 | Warnings, Adverse reactions | 70860-211-41 70860-211 70860021141 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.