NDC11 68001061025
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 |
|---|---|
| 68001-0610-25 | 68001-0610 |
| 68001-610-25 | 68001-610 |
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 | BluePoint Laboratories | f433c13c-dd8c-4dca-834e-a4ecf09d1eab | 2025-09-03 | Warnings, Adverse reactions | 68001-610-25 68001-610 68001061025 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.