NDC11 24979072507
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 |
|---|---|
| 24979-0725-07 | 24979-0725 |
| 24979-0725-7 | 24979-0725 |
| 24979-725-07 | 24979-725 |
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 |
|---|---|---|---|---|---|---|
| Anastrozole | ANASTROZOLE TABLETS | Upsher-Smith Laboratories, LLC | 7e0bd2cc-d3cc-403f-a6b6-4597ccb2f685 | 2025-07-09 | Warnings, Adverse reactions | 24979-725-07 24979-725 24979072507 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.