NDC11 70700028498
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 |
|---|---|
| 70700-0284-98 | 70700-0284 |
| 70700-284-98 | 70700-284 |
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 | Xiromed, LLC | 840cd7c0-9f33-f74e-f136-de7fe899bfb4 | 2021-10-04 | Warnings, Adverse reactions | 70700-284-98 70700-284 70700028498 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.