NDC11 25021082687
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 |
|---|---|
| 25021-0826-87 | 25021-0826 |
| 25021-826-87 | 25021-826 |
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 |
|---|---|---|---|---|---|---|
| zoledronic acid | ZOLEDRONIC ACID | Sagent Pharmaceuticals | 567578e6-cd2d-4339-b0f6-7a15444c0639 | 2025-03-11 | Warnings, Adverse reactions | 25021-826-87 25021-826 25021082687 |
| zoledronic acid | ZOLEDRONIC ACID | Sagent Pharmaceuticals | deb89be7-f40e-4fd4-a2cb-96634b45da84 | 2021-09-20 | Warnings, Adverse reactions | 25021-826 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.