NDC11 00310072010
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 |
|---|---|
| 00310-0720-10 | 00310-0720 |
| 00310-720-10 | 00310-720 |
| 0310-0720-10 | 0310-0720 |
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 |
|---|---|---|---|---|---|---|
| FASLODEX | FULVESTRANT | AstraZeneca Pharmaceuticals LP | 83d7a440-e904-4e36-afb5-cb02b1c919f7 | 2020-09-25 | Warnings, Adverse reactions | 0310-0720-10 0310-0720 00310072010 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.